Item | Value |
---|---|
geneid | 79033 |
ensemblid | ENSG00000117419.16 |
hgncid | 17276 |
symbol | ERI3 |
name | ERI1 exoribonuclease family member 3 |
refseq_nuc | NM_024066.3 |
refseq_prot | NP_076971.1 |
ensembl_nuc | ENST00000372257.7 |
ensembl_prot | ENSP00000361331.2 |
mane_status | MANE Select |
chr | chr1 |
start | 44221070 |
end | 44355257 |
strand | - |
ver | v1.2 |
region | chr1:44221070-44355257 |
region5000 | chr1:44216070-44360257 |
regionname0 | ERI3_chr1_44221070_44355257 |
regionname5000 | ERI3_chr1_44216070_44360257 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1011 | 337 | 84 | 60 | 153 | 8 | 30 | ERI3_chr1_44216070_44360257 | ERI3 | ATGGC others(1006): Show |
chr1 | 44216070 | 44360257 | ||
a0001c0002 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | ATGGC others(1006): Show |
chr1 | 44216070 | 44360257 | ||
a0001c0003 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | ATGGC others(1006): Show |
chr1 | 44216070 | 44360257 | ||
a0001c0004 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | ATGGC others(1006): Show |
chr1 | 44216070 | 44360257 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1733 | 330 | 79 | 60 | 151 | 8 | 30 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0001t0002 | 0/0 | 1733 | 3 | 3 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0001t0003 | 0/0 | 1733 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0001t0004 | 0/0 | 1733 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0001t0005 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0001t0006 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0002t0001 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0003t0001 | 0/0 | 1733 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
a0001c0004t0001 | 0/0 | 1733 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | GAGTC others(1728): Show |
chr1 | 44216070 | 44360257 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0330 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0001t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0337 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18968 | hp2 | a0001 | c0004 | t0001 | g0257 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | GIH | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | USA | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0139 | REF | REF | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0330 | REF | REF | ERI3_chr1_44216070_44360257 | ERI3 | chr1 | 44216070 | 44360257 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:44221564 | C | T | 1 | a0001c0002 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1008G>A | p.Pro336Pro | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 1239/1733 | 1008/1014 | 336/337 | chr1 | 44221564 | |||
chr1:44308357 | G | A | 1 | a0001c0003 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.711C>T | p.Asn237Asn | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/9 | 942/1733 | 711/1014 | 237/337 | chr1 | 44308357 | |||
chr1:44319721 | T | C | 1 | a0001c0004 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.513A>G | p.Leu171Leu | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/9 | 744/1733 | 513/1014 | 171/337 | chr1 | 44319721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:44221123 | G | A | 1 | a0001c0001t0004 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 435 | chr1 | 44221123 | ||||||
chr1:44221232 | G | C | 1 | a0001c0001t0002 | 3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 326 | chr1 | 44221232 | ||||||
chr1:44221284 | C | A | 1 | a0001c0001t0005 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 274 | chr1 | 44221284 | ||||||
chr1:44221365 | C | T | 1 | a0001c0001t0003 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 9/9 | 193 | chr1 | 44221365 | ||||||
chr1:44355222 | G | A | 1 | a0001c0001t0006 | 1 | HG02572.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-196C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/9 | chr1 | 44355222 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:44221880 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.932-240G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44221880 | |||||||
chr1:44221885 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-245A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44221885 | |||||||
chr1:44222242 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.932-602T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222242 | |||||||
chr1:44222366 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932-726G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222366 | |||||||
chr1:44222434 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.932-794G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222434 | |||||||
chr1:44222570 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.932-930A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222570 | |||||||
chr1:44222604 | G | C | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-964C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222604 | |||||||
chr1:44222607 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.932-967C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222607 | |||||||
chr1:44222749 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.932-1109G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222749 | |||||||
chr1:44222857 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932-1217C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222857 | |||||||
chr1:44222891 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.932-1251G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44222891 | |||||||
chr1:44223015 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.932-1375G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223015 | |||||||
chr1:44223198 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.932-1558C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223198 | |||||||
chr1:44223209 | C | T | 4 | a0001c0001t0001g0238 a0001c0001t0001g0270 a0001c0001t0001g0292 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1569G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223209 | |||||||
chr1:44223217 | G | A | 16 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0161 others(13): Show |
16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.932-1577C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223217 | |||||||
chr1:44223243 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.932-1603G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223243 | |||||||
chr1:44223311 | G | C | 1 | a0001c0002t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.932-1671C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223311 | |||||||
chr1:44223444 | A | C | 3 | a0001c0001t0001g0270 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | HG02109.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.932-1804T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223444 | |||||||
chr1:44223534 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0161 a0001c0001t0001g0165 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1894A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223534 | |||||||
chr1:44223578 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.932-1938C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223578 | |||||||
chr1:44223621 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-1981A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223621 | |||||||
chr1:44223763 | C | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-2123G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223763 | |||||||
chr1:44223789 | T | A | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.932-2149A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223789 | |||||||
chr1:44223825 | C | T | 16 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0161 others(13): Show |
16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.932-2185G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223825 | |||||||
chr1:44223934 | T | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.932-2294A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223934 | |||||||
chr1:44223937 | A | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-2297T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223937 | |||||||
chr1:44223955 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.932-2315T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223955 | |||||||
chr1:44223960 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.932-2320C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44223960 | |||||||
chr1:44224317 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.932-2677G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44224317 | |||||||
chr1:44224484 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0204 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-2844G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44224484 | |||||||
chr1:44224496 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0146 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-2856T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44224496 | |||||||
chr1:44225380 | G | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-3740C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225380 | |||||||
chr1:44225464 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.932-3824T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225464 | |||||||
chr1:44225663 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.932-4023G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225663 | |||||||
chr1:44225663 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-4023G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225663 | |||||||
chr1:44225860 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.932-4220T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44225860 | |||||||
chr1:44226534 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.932-4894A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226534 | |||||||
chr1:44226676 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-5036A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226676 | |||||||
chr1:44226741 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.932-5101A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226741 | |||||||
chr1:44226778 | A | AAC | 18 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0032 others(15): Show |
18 | HG00621.hp2 HG00738.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.932-5140_932-5139d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACAC | 38 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0124 others(35): Show |
39 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.932-5142_932-5139d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACACAC | 44 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0206 others(41): Show |
45 | HG00438.hp2 HG00544.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.932-5144_932-5139d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACACACA others(1): Show |
55 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(52): Show |
55 | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.932-5146_932-5139d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACACACA others(3): Show |
22 | a0001c0001t0001g0126 a0001c0001t0001g0151 a0001c0001t0001g0152 others(19): Show |
22 | HG00673.hp2 HG01978.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.932-5148_932-5139d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACACACA others(5): Show |
6 | a0001c0001t0001g0098 a0001c0001t0001g0158 a0001c0001t0001g0199 others(3): Show |
6 | HG00639.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-5150_932-5139d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACACACA others(7): Show |
1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.932-5152_932-5139d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | A | AACACACA others(9): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0116 |
2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.932-5154_932-5139d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | AAC | A | 24 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(21): Show |
24 | HG00280.hp1 HG00280.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.932-5140_932-5139d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226778 | AACAC | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0122 a0001c0001t0001g0128 others(22): Show |
25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.932-5142_932-5139d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226778 | |||||||
chr1:44226816 | A | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.932-5176T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44226816 | |||||||
chr1:44227113 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(86): Show |
90 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.932-5473G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227113 | |||||||
chr1:44227200 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-5560G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227200 | |||||||
chr1:44227474 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.932-5834C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227474 | |||||||
chr1:44227558 | AT | A | 28 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.932-5919delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227558 | |||||||
chr1:44227574 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-5934T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227574 | |||||||
chr1:44227753 | C | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0299 others(1): Show |
4 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-6113G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44227753 | |||||||
chr1:44228043 | A | G | 140 | a0001c0001t0001g0060 a0001c0001t0001g0095 a0001c0001t0001g0096 others(137): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.932-6403T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228043 | |||||||
chr1:44228093 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.932-6453C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228093 | |||||||
chr1:44228111 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.932-6471C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228111 | |||||||
chr1:44228301 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0220 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.932-6661C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228301 | |||||||
chr1:44228682 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.932-7042T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228682 | |||||||
chr1:44228804 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0108 others(1): Show |
4 | HG01261.hp1 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-7164C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228804 | |||||||
chr1:44228918 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.932-7278C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228918 | |||||||
chr1:44228991 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.932-7351G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44228991 | |||||||
chr1:44229205 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0006g0337 |
3 | HG00642.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.932-7565C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229205 | |||||||
chr1:44229509 | C | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0231 |
3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.932-7869G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229509 | |||||||
chr1:44229618 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0236 |
2 | HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.932-7978C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229618 | |||||||
chr1:44229632 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.932-7992C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229632 | |||||||
chr1:44229642 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.932-8002A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229642 | |||||||
chr1:44229650 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.932-8010G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229650 | |||||||
chr1:44229690 | G | C | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-8050C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229690 | |||||||
chr1:44229698 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932-8058C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229698 | |||||||
chr1:44229751 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.932-8111C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229751 | |||||||
chr1:44229796 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.932-8156G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229796 | |||||||
chr1:44229928 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-8288G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229928 | |||||||
chr1:44229985 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.932-8345G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229985 | |||||||
chr1:44229986 | G | A | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-8346C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44229986 | |||||||
chr1:44230116 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.932-8476T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230116 | |||||||
chr1:44230185 | A | G | 12 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0170 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-8545T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230185 | |||||||
chr1:44230273 | C | T | 12 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0170 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-8633G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230273 | |||||||
chr1:44230301 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.932-8661T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230301 | |||||||
chr1:44230316 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.932-8676G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230316 | |||||||
chr1:44230495 | G | T | 33 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0132 others(30): Show |
33 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.932-8855C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230495 | |||||||
chr1:44230610 | C | T | 26 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.932-8970G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44230610 | |||||||
chr1:44231379 | C | T | 3 | a0001c0001t0001g0329 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG01167.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.932-9739G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231379 | |||||||
chr1:44231583 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.932-9943C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231583 | |||||||
chr1:44231642 | G | A | 1 | a0001c0003t0001g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.932-10002C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231642 | |||||||
chr1:44231669 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.932-10029G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231669 | |||||||
chr1:44231764 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.932-10124G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231764 | |||||||
chr1:44231844 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG00423.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.932-10204G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44231844 | |||||||
chr1:44232001 | A | T | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-10361T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232001 | |||||||
chr1:44232065 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.932-10425C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232065 | |||||||
chr1:44232084 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.932-10444G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232084 | |||||||
chr1:44232499 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0087 |
2 | HG00621.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.932-10859T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232499 | |||||||
chr1:44232536 | ACTT | A | 16 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0161 others(13): Show |
16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.932-10899_932-1089 others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232536 | |||||||
chr1:44232813 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.932-11173G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232813 | |||||||
chr1:44232917 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.932-11277A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232917 | |||||||
chr1:44232924 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-11284C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44232924 | |||||||
chr1:44233401 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.932-11761G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233401 | |||||||
chr1:44233405 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.932-11765G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233405 | |||||||
chr1:44233405 | C | CT | 6 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0174 others(3): Show |
6 | HG01167.hp1 HG02040.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-11766dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233405 | |||||||
chr1:44233507 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.932-11867C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233507 | |||||||
chr1:44233684 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.932-12044A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233684 | |||||||
chr1:44233882 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.932-12242C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44233882 | |||||||
chr1:44234010 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0114 |
2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.932-12370C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234010 | |||||||
chr1:44234176 | T | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(86): Show |
90 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.932-12536A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234176 | |||||||
chr1:44234190 | CCAATAAT others(30): Show |
C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-12587_932-1255 others(41): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234190 | |||||||
chr1:44234440 | A | C | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-12800T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234440 | |||||||
chr1:44234632 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.932-12992G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234632 | |||||||
chr1:44234852 | C | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0049 others(2): Show |
5 | NA18962.hp2 NA18971.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+13087G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44234852 | |||||||
chr1:44235118 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.931+12821C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235118 | |||||||
chr1:44235468 | C | T | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+12471G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235468 | |||||||
chr1:44235533 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931+12406A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235533 | |||||||
chr1:44235542 | G | T | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.931+12397C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235542 | |||||||
chr1:44235605 | C | G | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.931+12334G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235605 | |||||||
chr1:44235745 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+12194A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44235745 | |||||||
chr1:44236185 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.931+11754G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236185 | |||||||
chr1:44236256 | T | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0170 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+11683A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236256 | |||||||
chr1:44236268 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0194 |
2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.931+11671G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236268 | |||||||
chr1:44236580 | G | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+11359C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236580 | |||||||
chr1:44236907 | G | A | 11 | a0001c0001t0001g0137 a0001c0001t0001g0142 a0001c0001t0001g0143 others(8): Show |
11 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+11032C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236907 | |||||||
chr1:44236951 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(91): Show |
95 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.931+10988G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44236951 | |||||||
chr1:44237043 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+10896C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237043 | |||||||
chr1:44237231 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.931+10708A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237231 | |||||||
chr1:44237637 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.931+10302G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237637 | |||||||
chr1:44237704 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.931+10235G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237704 | |||||||
chr1:44237706 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.931+10233C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237706 | |||||||
chr1:44237707 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.931+10232T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44237707 | |||||||
chr1:44238036 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+9903T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238036 | |||||||
chr1:44238196 | C | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+9743G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238196 | |||||||
chr1:44238277 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.931+9662C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238277 | |||||||
chr1:44238358 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.931+9581T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238358 | |||||||
chr1:44238372 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9567G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238372 | |||||||
chr1:44238531 | G | C | 6 | a0001c0001t0001g0131 a0001c0001t0001g0148 a0001c0001t0001g0152 others(3): Show |
6 | HG01071.hp1 HG01361.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+9408C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238531 | |||||||
chr1:44238569 | C | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+9370G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238569 | |||||||
chr1:44238636 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.931+9303G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238636 | |||||||
chr1:44238755 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.931+9184T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44238755 | |||||||
chr1:44239039 | C | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+8900G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239039 | |||||||
chr1:44239104 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | NA18965.hp2 NA18981.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+8835C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239104 | |||||||
chr1:44239226 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931+8713C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239226 | |||||||
chr1:44239270 | A | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+8669T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239270 | |||||||
chr1:44239550 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.931+8389G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239550 | |||||||
chr1:44239716 | C | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.931+8223G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239716 | |||||||
chr1:44239782 | A | AAGAGGAG others(2): Show |
4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+8148_931+8156d others(11): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44239782 | |||||||
chr1:44240013 | C | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02572.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.931+7926G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240013 | |||||||
chr1:44240127 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.931+7812C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240127 | |||||||
chr1:44240159 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.931+7780C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240159 | |||||||
chr1:44240330 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.931+7609C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240330 | |||||||
chr1:44240440 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.931+7499C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240440 | |||||||
chr1:44240441 | C | T | 16 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0161 others(13): Show |
16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.931+7498G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44240441 | |||||||
chr1:44241396 | T | G | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.931+6543A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241396 | |||||||
chr1:44241534 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+6405G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241534 | |||||||
chr1:44241556 | C | G | 1 | a0001c0001t0006g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.931+6383G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241556 | |||||||
chr1:44241608 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.931+6331C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241608 | |||||||
chr1:44241623 | G | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0060 others(243): Show |
248 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.931+6316C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241623 | |||||||
chr1:44241739 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.931+6200G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241739 | |||||||
chr1:44241805 | C | CACAT | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
171 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.931+6130_931+6133d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | |||||||
chr1:44241805 | C | CACATACA others(1): Show |
22 | a0001c0001t0001g0100 a0001c0001t0001g0119 a0001c0001t0001g0125 others(19): Show |
22 | HG00280.hp1 HG00438.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.931+6126_931+6133d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | |||||||
chr1:44241805 | C | CACATACA others(5): Show |
3 | a0001c0001t0001g0065 a0001c0001t0001g0170 a0001c0001t0001g0262 |
3 | HG00423.hp2 HG01884.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.931+6122_931+6133d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | |||||||
chr1:44241805 | CACAT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
55 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.931+6130_931+6133d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | |||||||
chr1:44241805 | CACATACA others(5): Show |
C | 2 | a0001c0001t0001g0301 a0001c0004t0001g0257 |
2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.931+6122_931+6133d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241805 | |||||||
chr1:44241866 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0081 |
3 | HG01255.hp2 HG01517.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.931+6073G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241866 | |||||||
chr1:44241963 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.931+5976G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44241963 | |||||||
chr1:44242096 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.931+5843C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242096 | |||||||
chr1:44242256 | G | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0210 |
2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.931+5683C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242256 | |||||||
chr1:44242320 | C | G | 1 | a0001c0001t0001g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.931+5619G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242320 | |||||||
chr1:44242373 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.931+5566T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242373 | |||||||
chr1:44242473 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.931+5466G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242473 | |||||||
chr1:44242618 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.931+5321C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242618 | |||||||
chr1:44242694 | A | AC | 5 | a0001c0001t0001g0059 a0001c0001t0001g0130 a0001c0001t0001g0169 others(2): Show |
5 | HG01433.hp2 HG02145.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+5244dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242694 | |||||||
chr1:44242711 | A | G | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.931+5228T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242711 | |||||||
chr1:44242796 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.931+5143C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242796 | |||||||
chr1:44242934 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.931+5005C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44242934 | |||||||
chr1:44243233 | AC | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+4705delG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243233 | |||||||
chr1:44243314 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931+4625C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243314 | |||||||
chr1:44243546 | G | A | 26 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.931+4393C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243546 | |||||||
chr1:44243752 | C | T | 7 | a0001c0001t0001g0126 a0001c0001t0001g0188 a0001c0001t0001g0195 others(4): Show |
7 | HG00621.hp1 HG02738.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+4187G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243752 | |||||||
chr1:44243773 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+4166G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44243773 | |||||||
chr1:44244125 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.931+3814A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244125 | |||||||
chr1:44244385 | A | G | 140 | a0001c0001t0001g0060 a0001c0001t0001g0095 a0001c0001t0001g0096 others(137): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.931+3554T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244385 | |||||||
chr1:44244421 | C | T | 70 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.931+3518G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244421 | |||||||
chr1:44244559 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.931+3380C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244559 | |||||||
chr1:44244692 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+3247C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244692 | |||||||
chr1:44244811 | C | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.931+3128G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44244811 | |||||||
chr1:44245097 | G | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+2842C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245097 | |||||||
chr1:44245151 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(101): Show |
106 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.931+2788G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245151 | |||||||
chr1:44245624 | T | C | 6 | a0001c0001t0001g0242 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00544.hp2 HG01167.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+2315A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245624 | |||||||
chr1:44245709 | T | C | 139 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(136): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.931+2230A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245709 | |||||||
chr1:44245719 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+2220T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245719 | |||||||
chr1:44245745 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.931+2194T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245745 | |||||||
chr1:44245924 | T | A | 1 | a0001c0001t0001g0325 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.931+2015A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44245924 | |||||||
chr1:44246252 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.931+1687A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246252 | |||||||
chr1:44246425 | G | A | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+1514C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246425 | |||||||
chr1:44246434 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.931+1505C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246434 | |||||||
chr1:44246485 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931+1454G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246485 | |||||||
chr1:44246613 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+1326A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246613 | |||||||
chr1:44246747 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.931+1192A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246747 | |||||||
chr1:44246799 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.931+1140T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246799 | |||||||
chr1:44246898 | C | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+1041G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246898 | |||||||
chr1:44246899 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.931+1040G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44246899 | |||||||
chr1:44247398 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931+541G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247398 | |||||||
chr1:44247471 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.931+468G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247471 | |||||||
chr1:44247641 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.931+298A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247641 | |||||||
chr1:44247795 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.931+144G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 8/8 | chr1 | 44247795 | |||||||
chr1:44248128 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.832-90A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248128 | |||||||
chr1:44248310 | C | T | 16 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0161 others(13): Show |
16 | HG01943.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-272G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248310 | |||||||
chr1:44248396 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.832-358G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248396 | |||||||
chr1:44248702 | A | AGT | 12 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0070 others(9): Show |
12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-666_832-665dup others(2): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | |||||||
chr1:44248702 | A | AGTGTGTG others(1): Show |
58 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0125 others(55): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.832-672_832-665dup others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | |||||||
chr1:44248702 | A | AGTGTGTG others(3): Show |
46 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0132 others(43): Show |
46 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.832-674_832-665dup others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | |||||||
chr1:44248702 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.832-676_832-665dup others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | |||||||
chr1:44248702 | AGT | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0329 a0001c0001t0001g0331 |
3 | HG01167.hp1 HG01261.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.832-666_832-665del others(2): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248702 | |||||||
chr1:44248882 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.832-844G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248882 | |||||||
chr1:44248932 | G | GC | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-895_832-894ins others(1): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248932 | |||||||
chr1:44248960 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-922C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44248960 | |||||||
chr1:44249220 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-1182C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249220 | |||||||
chr1:44249325 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-1287C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249325 | |||||||
chr1:44249580 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.832-1542T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249580 | |||||||
chr1:44249874 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-1836G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249874 | |||||||
chr1:44249930 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.832-1892G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249930 | |||||||
chr1:44249948 | G | A | 26 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.832-1910C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249948 | |||||||
chr1:44249960 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-1922A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249960 | |||||||
chr1:44249989 | G | A | 6 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-1951C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44249989 | |||||||
chr1:44250165 | T | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.832-2127A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250165 | |||||||
chr1:44250202 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-2164C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250202 | |||||||
chr1:44250268 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-2230A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250268 | |||||||
chr1:44250299 | G | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.832-2261C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250299 | |||||||
chr1:44250476 | G | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.832-2438C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250476 | |||||||
chr1:44250529 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.832-2491C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250529 | |||||||
chr1:44250658 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.832-2620T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250658 | |||||||
chr1:44250734 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.832-2696C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250734 | |||||||
chr1:44250928 | C | T | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-2890G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250928 | |||||||
chr1:44250939 | C | G | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-2901G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250939 | |||||||
chr1:44250957 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.832-2919G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44250957 | |||||||
chr1:44251193 | A | AC | 6 | a0001c0001t0001g0059 a0001c0001t0001g0090 a0001c0001t0001g0100 others(3): Show |
6 | HG00438.hp2 HG01261.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-3156dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251193 | |||||||
chr1:44251229 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.832-3191G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251229 | |||||||
chr1:44251239 | G | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG01167.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.832-3201C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251239 | |||||||
chr1:44251337 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0231 |
3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.832-3299C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251337 | |||||||
chr1:44251586 | G | A | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-3548C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251586 | |||||||
chr1:44251597 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-3559T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251597 | |||||||
chr1:44251778 | T | C | 140 | a0001c0001t0001g0060 a0001c0001t0001g0095 a0001c0001t0001g0096 others(137): Show |
140 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.832-3740A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251778 | |||||||
chr1:44251904 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.832-3866C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251904 | |||||||
chr1:44251932 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-3894C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251932 | |||||||
chr1:44251980 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0158 a0001c0001t0001g0228 others(83): Show |
87 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.832-3942G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44251980 | |||||||
chr1:44252247 | G | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-4209C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44252247 | |||||||
chr1:44252390 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.832-4352A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44252390 | |||||||
chr1:44252627 | C | T | 24 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0148 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-4589G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44252627 | |||||||
chr1:44253066 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.832-5028C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253066 | |||||||
chr1:44253581 | C | G | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | NA18959.hp1 NA18970.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-5543G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253581 | |||||||
chr1:44253709 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.832-5671T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253709 | |||||||
chr1:44253718 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.832-5680C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44253718 | |||||||
chr1:44254249 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.832-6211A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44254249 | |||||||
chr1:44254409 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.832-6371T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44254409 | |||||||
chr1:44254657 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.832-6619G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44254657 | |||||||
chr1:44255034 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-6996A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255034 | |||||||
chr1:44255311 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.832-7273A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255311 | |||||||
chr1:44255315 | T | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.832-7277A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255315 | |||||||
chr1:44255319 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.832-7281A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255319 | |||||||
chr1:44255562 | A | C | 10 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0155 others(7): Show |
10 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-7524T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255562 | |||||||
chr1:44255747 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0006g0337 |
3 | HG00642.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.832-7709G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255747 | |||||||
chr1:44255803 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.832-7765A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255803 | |||||||
chr1:44255830 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.832-7792A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44255830 | |||||||
chr1:44256067 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0041 others(105): Show |
110 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.832-8029C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44256067 | |||||||
chr1:44256215 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-8177G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44256215 | |||||||
chr1:44256796 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.832-8758C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44256796 | |||||||
chr1:44257165 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.832-9127G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44257165 | |||||||
chr1:44257274 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.832-9236A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44257274 | |||||||
chr1:44258072 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832-10034C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258072 | |||||||
chr1:44258215 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.832-10177T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258215 | |||||||
chr1:44258350 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-10312G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258350 | |||||||
chr1:44258530 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0006g0337 |
2 | HG00642.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832-10492G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258530 | |||||||
chr1:44258543 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-10505A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258543 | |||||||
chr1:44258640 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.832-10602G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258640 | |||||||
chr1:44258672 | G | C | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-10634C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258672 | |||||||
chr1:44258906 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-10868G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258906 | |||||||
chr1:44258961 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832-10923G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44258961 | |||||||
chr1:44259064 | T | G | 12 | a0001c0001t0001g0060 a0001c0001t0001g0135 a0001c0001t0001g0170 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-11026A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259064 | |||||||
chr1:44259106 | C | T | 138 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(135): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.832-11068G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259106 | |||||||
chr1:44259116 | A | G | 78 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(75): Show |
78 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.832-11078T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259116 | |||||||
chr1:44259340 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.832-11302C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259340 | |||||||
chr1:44259558 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(4): Show |
7 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-11520G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259558 | |||||||
chr1:44259640 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.832-11602C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259640 | |||||||
chr1:44259681 | A | AACAC | 3 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 |
3 | NA18943.hp1 NA18951.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.832-11647_832-1164 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259681 | |||||||
chr1:44259689 | G | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0048 others(1): Show |
4 | NA18943.hp1 NA18951.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-11651C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GAC | 22 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0044 others(19): Show |
22 | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.832-11653_832-1165 others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACAC | 3 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0001t0001g0333 |
3 | HG00642.hp2 HG02717.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.832-11655_832-1165 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACAC | 32 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(29): Show |
33 | HG00642.hp1 HG01169.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.832-11657_832-1165 others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(1): Show |
37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
37 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.832-11659_832-1165 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(3): Show |
23 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0035 others(20): Show |
23 | HG00544.hp1 HG01167.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.832-11661_832-1165 others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(5): Show |
28 | a0001c0001t0001g0060 a0001c0001t0001g0120 a0001c0001t0001g0135 others(25): Show |
29 | HG00738.hp1 HG01516.hp2 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.832-11663_832-1165 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(7): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0102 others(49): Show |
53 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.832-11665_832-1165 others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(9): Show |
31 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0103 others(28): Show |
31 | HG00280.hp2 HG00733.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-11667_832-1165 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(11): Show |
15 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0101 others(12): Show |
15 | HG01884.hp1 HG01978.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-11669_832-1165 others(22): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(13): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0121 others(1): Show |
4 | HG02027.hp2 HG03139.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-11671_832-1165 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(15): Show |
3 | a0001c0001t0001g0163 a0001c0001t0001g0205 a0001c0001t0001g0222 |
3 | HG02622.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.832-11673_832-1165 others(26): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(17): Show |
1 | a0001c0001t0001g0115 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.832-11675_832-1165 others(28): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | G | GACACACA others(9): Show |
4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-11652_832-1165 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259689 | GACACAC | G | 66 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(63): Show |
66 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.832-11657_832-1165 others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259689 | |||||||
chr1:44259724 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.832-11687_832-1168 others(17): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259724 | |||||||
chr1:44259724 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.832-11687_832-1168 others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259724 | |||||||
chr1:44259724 | A | ACACACAC others(12): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0112 |
2 | HG01261.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.832-11687_832-1168 others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259724 | |||||||
chr1:44259871 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.832-11833G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259871 | |||||||
chr1:44259875 | C | CTAGA | 72 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(69): Show |
72 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.832-11841_832-1183 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | C | CTAGATAG others(1): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(23): Show |
27 | HG00423.hp2 HG00673.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.832-11845_832-1183 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | C | CTAGATAG others(5): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0274 |
2 | HG02004.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.832-11849_832-1183 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | C | CTAGATAG others(9): Show |
2 | a0001c0001t0001g0279 a0001c0001t0001g0306 |
2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.832-11853_832-1183 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | C | CTAGATAG others(21): Show |
1 | a0001c0001t0001g0010 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.832-11865_832-1183 others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | CTAGA | C | 9 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0179 others(6): Show |
9 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-11841_832-1183 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | CTAGATAG others(1): Show |
C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0110 a0001c0001t0001g0116 others(3): Show |
6 | HG00642.hp1 HG01255.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-11845_832-1183 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259875 | CTAGATAG others(5): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.832-11849_832-1183 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259875 | |||||||
chr1:44259876 | T | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.832-11838A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259876 | |||||||
chr1:44259912 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0170 a0001c0001t0001g0171 others(7): Show |
10 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-11874A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259912 | |||||||
chr1:44259912 | T | TAGAC | 4 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-11875_832-1187 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259912 | |||||||
chr1:44259916 | T | C | 16 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0167 others(13): Show |
16 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-11878A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | |||||||
chr1:44259916 | T | TAGAC | 8 | a0001c0001t0001g0141 a0001c0001t0001g0161 a0001c0001t0001g0209 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-11879_832-1187 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | |||||||
chr1:44259916 | T | TAGACAGA others(1): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0331 a0001c0001t0001g0336 |
3 | HG01261.hp2 NA19056.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.832-11879_832-1187 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | |||||||
chr1:44259916 | T | TAGACAGA others(5): Show |
3 | a0001c0001t0001g0163 a0001c0001t0001g0205 a0001c0001t0001g0207 |
3 | HG02622.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.832-11879_832-1187 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259916 | |||||||
chr1:44259920 | T | C | 58 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0098 others(55): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.832-11882A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGAC | 35 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0101 others(32): Show |
36 | HG00558.hp2 HG01071.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.832-11886_832-1188 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGACAGA others(5): Show |
6 | a0001c0001t0001g0146 a0001c0001t0001g0165 a0001c0001t0001g0206 others(3): Show |
6 | HG02976.hp2 HG03041.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-11894_832-1188 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGACAGA others(9): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0166 |
2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.832-11898_832-1188 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(1): Show |
18 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0061 others(15): Show |
18 | HG00438.hp1 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.832-11883_832-1188 others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(5): Show |
11 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(8): Show |
11 | HG00280.hp2 HG01261.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-11883_832-1188 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(13): Show |
1 | a0001c0001t0001g0062 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.832-11883_832-1188 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(5): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0075 a0001c0001t0001g0251 others(4): Show |
7 | HG01516.hp2 HG01517.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-11883_832-1188 others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(9): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0283 |
2 | HG00738.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.832-11883_832-1188 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(9): Show |
2 | a0001c0001t0001g0267 a0001c0001t0001g0310 |
2 | HG03704.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.832-11883_832-1188 others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | T | TAGATAGA others(13): Show |
1 | a0001c0001t0001g0265 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.832-11883_832-1188 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259920 | TAGAC | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0300 |
3 | HG00408.hp1 HG01081.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.832-11886_832-1188 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259920 | |||||||
chr1:44259924 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0085 a0001c0001t0001g0117 others(4): Show |
7 | HG00733.hp2 HG02027.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-11886G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259924 | |||||||
chr1:44259980 | T | C | 9 | a0001c0001t0001g0247 a0001c0001t0001g0265 a0001c0001t0001g0271 others(6): Show |
9 | HG01358.hp2 HG01496.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-11942A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44259980 | |||||||
chr1:44260211 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0060 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.832-12173A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260211 | |||||||
chr1:44260244 | C | G | 139 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(136): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.832-12206G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260244 | |||||||
chr1:44260284 | G | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-12246C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260284 | |||||||
chr1:44260348 | T | C | 24 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0148 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-12310A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260348 | |||||||
chr1:44260424 | C | G | 21 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
21 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-12386G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260424 | |||||||
chr1:44260682 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.832-12644A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260682 | |||||||
chr1:44260979 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.832-12941G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260979 | |||||||
chr1:44260998 | GTT | G | 26 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.832-12962_832-1296 others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44260998 | |||||||
chr1:44261281 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0161 a0001c0001t0001g0165 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-13243C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261281 | |||||||
chr1:44261631 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.832-13593C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261631 | |||||||
chr1:44261769 | A | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-13731T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261769 | |||||||
chr1:44261906 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-13868T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261906 | |||||||
chr1:44261940 | T | C | 98 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(95): Show |
98 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.832-13902A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261940 | |||||||
chr1:44261999 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0080 |
3 | NA18997.hp1 NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.832-13961C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44261999 | |||||||
chr1:44262124 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.832-14086C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262124 | |||||||
chr1:44262290 | C | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0108 |
3 | HG01261.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.832-14252G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262290 | |||||||
chr1:44262329 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-14291C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262329 | |||||||
chr1:44262422 | C | G | 1 | a0001c0001t0003g0020 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.832-14384G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262422 | |||||||
chr1:44262472 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.832-14434A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262472 | |||||||
chr1:44262572 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832-14534C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262572 | |||||||
chr1:44262645 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.832-14607C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262645 | |||||||
chr1:44262759 | G | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-14721C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262759 | |||||||
chr1:44262892 | T | C | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-14854A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44262892 | |||||||
chr1:44263076 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.832-15038T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263076 | |||||||
chr1:44263515 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.832-15477C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263515 | |||||||
chr1:44263596 | T | A | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.832-15558A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263596 | |||||||
chr1:44263606 | A | C | 4 | a0001c0001t0001g0238 a0001c0001t0001g0270 a0001c0001t0001g0292 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-15568T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263606 | |||||||
chr1:44263685 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0166 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.832-15647T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263685 | |||||||
chr1:44263724 | C | T | 135 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(132): Show |
135 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.832-15686G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44263724 | |||||||
chr1:44264209 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-16171A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264209 | |||||||
chr1:44264264 | T | C | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-16226A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264264 | |||||||
chr1:44264296 | T | C | 139 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(136): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.832-16258A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264296 | |||||||
chr1:44264331 | C | T | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-16293G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264331 | |||||||
chr1:44264411 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.832-16373G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264411 | |||||||
chr1:44264617 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-16579G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264617 | |||||||
chr1:44264632 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-16594G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44264632 | |||||||
chr1:44265151 | G | GGAGA | 313 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(310): Show |
316 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.832-17117_832-1711 others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265151 | |||||||
chr1:44265304 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.832-17266C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265304 | |||||||
chr1:44265327 | A | C | 3 | a0001c0001t0001g0331 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG01261.hp2 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.832-17289T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265327 | |||||||
chr1:44265351 | G | A | 33 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0132 others(30): Show |
33 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.832-17313C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265351 | |||||||
chr1:44265396 | T | G | 139 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(136): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.832-17358A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265396 | |||||||
chr1:44265439 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832-17401G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265439 | |||||||
chr1:44265456 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.832-17418G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265456 | |||||||
chr1:44265587 | C | T | 24 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0148 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-17549G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265587 | |||||||
chr1:44265599 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.832-17561G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265599 | |||||||
chr1:44265653 | T | TA | 7 | a0001c0001t0001g0090 a0001c0001t0001g0224 a0001c0001t0001g0225 others(4): Show |
7 | HG01243.hp2 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-17616dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265653 | |||||||
chr1:44265707 | AGAAAT | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-17674_832-1767 others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44265707 | |||||||
chr1:44266267 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.832-18229T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266267 | |||||||
chr1:44266429 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.832-18391T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266429 | |||||||
chr1:44266506 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.831+18329A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266506 | |||||||
chr1:44266558 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.831+18277G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266558 | |||||||
chr1:44266785 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+18050C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44266785 | |||||||
chr1:44267129 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.831+17706C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267129 | |||||||
chr1:44267215 | C | T | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.831+17620G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267215 | |||||||
chr1:44267383 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0166 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.831+17452T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267383 | |||||||
chr1:44267433 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.831+17402C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267433 | |||||||
chr1:44267492 | C | T | 1 | a0001c0003t0001g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.831+17343G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267492 | |||||||
chr1:44267535 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0159 |
2 | HG01891.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.831+17300G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267535 | |||||||
chr1:44267579 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02572.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831+17256G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267579 | |||||||
chr1:44267644 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.831+17191T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267644 | |||||||
chr1:44267659 | TCTGCCTG others(12): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.831+17157_831+1717 others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267659 | |||||||
chr1:44267720 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.831+17115T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267720 | |||||||
chr1:44267775 | T | C | 11 | a0001c0001t0001g0111 a0001c0001t0001g0233 a0001c0001t0001g0234 others(8): Show |
11 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+17060A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267775 | |||||||
chr1:44267799 | A | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+17036T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267799 | |||||||
chr1:44267916 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+16919G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44267916 | |||||||
chr1:44268269 | A | AGGACTTC others(3): Show |
137 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(134): Show |
137 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.831+16565_831+1656 others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44268269 | |||||||
chr1:44268988 | G | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15847C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44268988 | |||||||
chr1:44269220 | G | A | 27 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(24): Show |
27 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.831+15615C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269220 | |||||||
chr1:44269523 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15312G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269523 | |||||||
chr1:44269529 | T | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+15306A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269529 | |||||||
chr1:44269620 | C | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0049 others(1): Show |
4 | NA18962.hp2 NA18971.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15215G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269620 | |||||||
chr1:44269677 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+15158T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269677 | |||||||
chr1:44269934 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.831+14901G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269934 | |||||||
chr1:44269951 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+14884C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44269951 | |||||||
chr1:44270235 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.831+14600G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270235 | |||||||
chr1:44270300 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.831+14535G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270300 | |||||||
chr1:44270409 | C | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831+14426G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270409 | |||||||
chr1:44270649 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+14186A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270649 | |||||||
chr1:44270945 | A | G | 1 | a0001c0002t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.831+13890T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44270945 | |||||||
chr1:44271002 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+13833G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271002 | |||||||
chr1:44271036 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0220 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.831+13799C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271036 | |||||||
chr1:44271056 | C | T | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+13779G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271056 | |||||||
chr1:44271291 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0288 |
2 | NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.831+13544G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271291 | |||||||
chr1:44271779 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+13056T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44271779 | |||||||
chr1:44272093 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+12742C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272093 | |||||||
chr1:44272393 | A | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+12442T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272393 | |||||||
chr1:44272613 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.831+12222C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272613 | |||||||
chr1:44272625 | C | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+12210G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272625 | |||||||
chr1:44272841 | A | AAAAAT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
141 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.831+11989_831+1199 others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | |||||||
chr1:44272841 | A | AAAAATAA others(3): Show |
28 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0242 others(25): Show |
28 | HG00438.hp2 HG00544.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.831+11984_831+1199 others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | |||||||
chr1:44272841 | A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0327 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.831+11979_831+1199 others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | |||||||
chr1:44272841 | A | AAAAATAA others(13): Show |
4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11974_831+1199 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | |||||||
chr1:44272841 | AAAAAT | A | 8 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(5): Show |
8 | HG01261.hp2 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+11989_831+1199 others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | |||||||
chr1:44272841 | AAAAATAA others(13): Show |
A | 15 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(12): Show |
15 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.831+11974_831+1199 others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272841 | |||||||
chr1:44272896 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+11939G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272896 | |||||||
chr1:44272899 | T | TA | 4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+11935dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272899 | |||||||
chr1:44272929 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11906A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272929 | |||||||
chr1:44272936 | T | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.831+11899A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44272936 | |||||||
chr1:44273003 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11832A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273003 | |||||||
chr1:44273171 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.831+11664G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273171 | |||||||
chr1:44273306 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.831+11529G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273306 | |||||||
chr1:44273370 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0161 a0001c0001t0001g0165 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11465G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273370 | |||||||
chr1:44273480 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.831+11355T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273480 | |||||||
chr1:44273498 | G | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(86): Show |
90 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.831+11337C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273498 | |||||||
chr1:44273669 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.831+11166C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273669 | |||||||
chr1:44273859 | G | C | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.831+10976C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273859 | |||||||
chr1:44273861 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG02257.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.831+10974G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44273861 | |||||||
chr1:44274233 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0204 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.831+10602A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274233 | |||||||
chr1:44274314 | A | G | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.831+10521T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274314 | |||||||
chr1:44274334 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+10501C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274334 | |||||||
chr1:44274352 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(240): Show |
245 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.831+10483A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274352 | |||||||
chr1:44274393 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.831+10442T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274393 | |||||||
chr1:44274572 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.831+10263T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274572 | |||||||
chr1:44274764 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.831+10071G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44274764 | |||||||
chr1:44275253 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0155 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.831+9582G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275253 | |||||||
chr1:44275651 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.831+9184G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275651 | |||||||
chr1:44275724 | T | C | 28 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.831+9111A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275724 | |||||||
chr1:44275896 | A | C | 139 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(136): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.831+8939T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275896 | |||||||
chr1:44275917 | A | AT | 4 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0108 others(1): Show |
4 | HG01261.hp1 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+8917dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275917 | |||||||
chr1:44275986 | G | A | 4 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0256 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+8849C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44275986 | |||||||
chr1:44276774 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831+8061C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44276774 | |||||||
chr1:44276888 | AGG | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+7945_831+7946d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44276888 | |||||||
chr1:44277044 | G | C | 10 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0155 others(7): Show |
10 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+7791C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277044 | |||||||
chr1:44277247 | A | G | 7 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0166 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7588T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277247 | |||||||
chr1:44277308 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.831+7527G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277308 | |||||||
chr1:44277310 | T | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+7525A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277310 | |||||||
chr1:44277473 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.831+7362T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277473 | |||||||
chr1:44277479 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.831+7356A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277479 | |||||||
chr1:44277735 | C | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+7100G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277735 | |||||||
chr1:44277834 | T | C | 7 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(4): Show |
7 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7001A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44277834 | |||||||
chr1:44278132 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+6703C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278132 | |||||||
chr1:44278375 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+6460C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278375 | |||||||
chr1:44278425 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.831+6410G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278425 | |||||||
chr1:44278477 | G | GA | 12 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0001g0110 others(9): Show |
12 | HG00642.hp1 HG01081.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+6357dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278477 | |||||||
chr1:44278477 | GAA | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+6356_831+6357d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278477 | |||||||
chr1:44278485 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.831+6350T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278485 | |||||||
chr1:44278597 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+6238A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278597 | |||||||
chr1:44278632 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.831+6203G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278632 | |||||||
chr1:44278693 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0240 others(11): Show |
15 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.831+6142C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278693 | |||||||
chr1:44278745 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.831+6090C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278745 | |||||||
chr1:44278761 | G | C | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+6074C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278761 | |||||||
chr1:44278784 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.831+6051T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278784 | |||||||
chr1:44278859 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+5976A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44278859 | |||||||
chr1:44279074 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.831+5761T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279074 | |||||||
chr1:44279075 | T | A | 1 | a0001c0001t0001g0090 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.831+5760A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279075 | |||||||
chr1:44279089 | G | T | 6 | a0001c0001t0001g0329 a0001c0001t0001g0331 a0001c0001t0001g0332 others(3): Show |
6 | HG01167.hp1 HG01261.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+5746C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279089 | |||||||
chr1:44279186 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+5649T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279186 | |||||||
chr1:44279217 | AATAACAC others(24): Show |
A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0069 others(2): Show |
5 | HG01071.hp2 HG01106.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+5587_831+5617d others(33): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279217 | |||||||
chr1:44279230 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.831+5605T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279230 | |||||||
chr1:44279432 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+5403G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279432 | |||||||
chr1:44279559 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.831+5276G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279559 | |||||||
chr1:44279778 | T | A | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.831+5057A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279778 | |||||||
chr1:44279936 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.831+4899T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279936 | |||||||
chr1:44279952 | C | T | 106 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0125 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.831+4883G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44279952 | |||||||
chr1:44280124 | C | T | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+4711G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280124 | |||||||
chr1:44280264 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831+4571A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280264 | |||||||
chr1:44280402 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0077 others(1): Show |
4 | HG01071.hp2 HG01106.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+4433C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280402 | |||||||
chr1:44280438 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.831+4397T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280438 | |||||||
chr1:44280530 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.831+4305A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280530 | |||||||
chr1:44280545 | G | A | 10 | a0001c0001t0001g0228 a0001c0001t0001g0251 a0001c0001t0001g0267 others(7): Show |
10 | HG00738.hp1 HG01256.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+4290C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280545 | |||||||
chr1:44280781 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.831+4054G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280781 | |||||||
chr1:44280781 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0009 |
2 | NA18944.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.831+4054G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280781 | |||||||
chr1:44280880 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.831+3955T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280880 | |||||||
chr1:44280995 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+3840G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44280995 | |||||||
chr1:44281005 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.831+3830T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281005 | |||||||
chr1:44281212 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.831+3623T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281212 | |||||||
chr1:44281254 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.831+3581C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281254 | |||||||
chr1:44281582 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+3253G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281582 | |||||||
chr1:44281588 | G | GA | 8 | a0001c0001t0001g0051 a0001c0001t0001g0090 a0001c0001t0001g0230 others(5): Show |
8 | HG01081.hp2 HG01175.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+3246dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | |||||||
chr1:44281588 | G | GAAA | 8 | a0001c0001t0001g0109 a0001c0001t0001g0164 a0001c0001t0001g0171 others(5): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+3244_831+3246d others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | |||||||
chr1:44281588 | G | GAAAAA | 6 | a0001c0001t0001g0127 a0001c0001t0001g0146 a0001c0001t0001g0161 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+3242_831+3246d others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | |||||||
chr1:44281588 | G | GAAAAAA | 19 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0137 others(16): Show |
19 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.831+3241_831+3246d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281588 | |||||||
chr1:44281599 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.831+3235_831+3236i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281599 | |||||||
chr1:44281601 | A | AAAAAAT | 7 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG00558.hp2 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+3233_831+3234i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0331 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.831+3233_831+3234i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | AAAT | 9 | a0001c0001t0001g0163 a0001c0001t0001g0168 a0001c0001t0001g0205 others(6): Show |
9 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | AAATAT | 7 | a0001c0001t0001g0134 a0001c0001t0001g0147 a0001c0001t0001g0157 others(4): Show |
7 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | AAATATAT | 16 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0001c0001t0001g0150 others(13): Show |
16 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | AATATATA others(3): Show |
3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02965.hp1 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.831+3224_831+3233d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | ATATATAT | 7 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
7 | HG01071.hp1 HG01361.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+3233_831+3234i others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281601 | A | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0082 others(20): Show |
23 | HG01071.hp2 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.831+3234T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281601 | |||||||
chr1:44281602 | AT | A | 17 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(14): Show |
17 | HG00280.hp2 HG02004.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+3232delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281602 | |||||||
chr1:44281603 | T | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0028 others(32): Show |
38 | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.831+3232A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281603 | |||||||
chr1:44281605 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.831+3230A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281605 | |||||||
chr1:44281619 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.831+3216A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281619 | |||||||
chr1:44281639 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.831+3196G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281639 | |||||||
chr1:44281721 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.831+3114G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281721 | |||||||
chr1:44281878 | A | ATG | 45 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0071 others(42): Show |
45 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.831+2955_831+2956d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | ATGTG | 30 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0099 others(27): Show |
31 | HG00280.hp1 HG00408.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.831+2953_831+2956d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | ATGTGTG | 17 | a0001c0001t0001g0117 a0001c0001t0001g0129 a0001c0001t0001g0134 others(14): Show |
17 | HG00738.hp1 HG01071.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.831+2951_831+2956d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0104 a0001c0001t0001g0112 a0001c0001t0001g0131 others(6): Show |
9 | HG01433.hp2 HG01934.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+2949_831+2956d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0177 |
3 | HG01952.hp1 HG01978.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.831+2947_831+2956d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+2945_831+2956d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0190 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.831+2943_831+2956d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.831+2957T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATG | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
76 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.831+2955_831+2956d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTG | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(15): Show |
20 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+2953_831+2956d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTGTG | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0001g0066 others(9): Show |
12 | HG00642.hp2 HG01517.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+2951_831+2956d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTGTGT others(1): Show |
A | 8 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+2949_831+2956d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTGTGT others(3): Show |
A | 11 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02486.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+2947_831+2956d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTGTGT others(5): Show |
A | 6 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+2945_831+2956d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0277 |
3 | HG01884.hp1 HG02922.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.831+2943_831+2956d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281878 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.831+2941_831+2956d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281878 | |||||||
chr1:44281926 | GTA | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0077 others(2): Show |
5 | HG01071.hp2 HG01106.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+2907_831+2908d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281926 | |||||||
chr1:44281928 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0227 |
3 | HG01243.hp2 HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.831+2907T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44281928 | |||||||
chr1:44282300 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0095 others(241): Show |
246 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.831+2535A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44282300 | |||||||
chr1:44282434 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.831+2401C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44282434 | |||||||
chr1:44283240 | C | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+1595G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283240 | |||||||
chr1:44283430 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.831+1405A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283430 | |||||||
chr1:44283464 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.831+1371T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283464 | |||||||
chr1:44283968 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+867G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283968 | |||||||
chr1:44283995 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+840G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44283995 | |||||||
chr1:44284209 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+626C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44284209 | |||||||
chr1:44284597 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(101): Show |
106 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.831+238C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44284597 | |||||||
chr1:44284817 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.831+18C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 7/8 | chr1 | 44284817 | |||||||
chr1:44285036 | T | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0205 a0001c0001t0001g0207 |
3 | HG02622.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.759-129A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285036 | |||||||
chr1:44285121 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.759-214C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285121 | |||||||
chr1:44285123 | C | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0178 others(2): Show |
5 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-216G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285123 | |||||||
chr1:44285356 | G | A | 28 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.759-449C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285356 | |||||||
chr1:44285381 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.759-474A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285381 | |||||||
chr1:44285382 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-475A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285382 | |||||||
chr1:44285534 | A | G | 106 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0125 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.759-627T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285534 | |||||||
chr1:44285577 | C | A | 1 | a0001c0001t0001g0309 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.759-670G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285577 | |||||||
chr1:44285659 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0060 others(242): Show |
247 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.759-752G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285659 | |||||||
chr1:44285704 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.759-797A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285704 | |||||||
chr1:44285718 | G | A | 137 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(134): Show |
137 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.759-811C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44285718 | |||||||
chr1:44286038 | T | C | 106 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0125 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.759-1131A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286038 | |||||||
chr1:44286278 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0288 |
2 | NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.759-1371G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286278 | |||||||
chr1:44286649 | C | G | 4 | a0001c0001t0001g0127 a0001c0001t0001g0161 a0001c0001t0001g0165 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-1742G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286649 | |||||||
chr1:44286897 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.759-1990T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44286897 | |||||||
chr1:44287115 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-2208C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287115 | |||||||
chr1:44287290 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.759-2383G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287290 | |||||||
chr1:44287294 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.759-2387A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287294 | |||||||
chr1:44287333 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.759-2426T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287333 | |||||||
chr1:44287365 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0030 |
3 | NA18995.hp1 NA19011.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.759-2458G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287365 | |||||||
chr1:44287431 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.759-2524G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287431 | |||||||
chr1:44287467 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.759-2560A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287467 | |||||||
chr1:44287528 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.759-2621C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287528 | |||||||
chr1:44287831 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-2924A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287831 | |||||||
chr1:44287839 | G | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0170 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.759-2932C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44287839 | |||||||
chr1:44288016 | C | T | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.759-3109G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288016 | |||||||
chr1:44288139 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.759-3232G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288139 | |||||||
chr1:44288150 | CCAGA | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
228 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.759-3247_759-3244d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288150 | |||||||
chr1:44288638 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759-3731G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288638 | |||||||
chr1:44288885 | T | G | 28 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.759-3978A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288885 | |||||||
chr1:44288916 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0111 others(97): Show |
101 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.759-4009T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288916 | |||||||
chr1:44288954 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.759-4047G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44288954 | |||||||
chr1:44289045 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759-4138A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289045 | |||||||
chr1:44289127 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.759-4220C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289127 | |||||||
chr1:44289342 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.759-4435C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289342 | |||||||
chr1:44289515 | A | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.759-4608T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289515 | |||||||
chr1:44289558 | T | C | 1 | a0001c0001t0005g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.759-4651A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289558 | |||||||
chr1:44289690 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.759-4783G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289690 | |||||||
chr1:44289890 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
233 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.759-4983A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289890 | |||||||
chr1:44289901 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.759-4994C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289901 | |||||||
chr1:44289987 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.759-5080A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44289987 | |||||||
chr1:44290100 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.759-5193C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290100 | |||||||
chr1:44290501 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-5594C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290501 | |||||||
chr1:44290645 | G | A | 6 | a0001c0001t0001g0247 a0001c0001t0001g0265 a0001c0001t0001g0271 others(3): Show |
6 | HG01358.hp2 HG01496.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-5738C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290645 | |||||||
chr1:44290804 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.759-5897C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290804 | |||||||
chr1:44290874 | G | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-5967C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290874 | |||||||
chr1:44290914 | A | T | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759-6007T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290914 | |||||||
chr1:44290958 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.759-6051T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290958 | |||||||
chr1:44290994 | G | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-6087C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44290994 | |||||||
chr1:44291075 | T | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
38 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.759-6168A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291075 | |||||||
chr1:44291355 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0124 |
3 | HG02572.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.759-6448G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291355 | |||||||
chr1:44291463 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0166 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.759-6556G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291463 | |||||||
chr1:44291733 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.759-6826C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291733 | |||||||
chr1:44291753 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.759-6846A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291753 | |||||||
chr1:44291806 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.759-6899C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291806 | |||||||
chr1:44291975 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0270 a0001c0001t0001g0292 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-7068C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44291975 | |||||||
chr1:44292365 | C | T | 10 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(7): Show |
10 | HG02027.hp1 HG02040.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.759-7458G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292365 | |||||||
chr1:44292644 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.759-7737C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292644 | |||||||
chr1:44292708 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.759-7801A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292708 | |||||||
chr1:44292734 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.759-7827G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44292734 | |||||||
chr1:44293060 | C | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-8153G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293060 | |||||||
chr1:44293342 | T | C | 1 | a0001c0001t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.759-8435A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293342 | |||||||
chr1:44293546 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.759-8639G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293546 | |||||||
chr1:44293547 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.759-8640C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293547 | |||||||
chr1:44293600 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.759-8693G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293600 | |||||||
chr1:44293716 | G | A | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-8809C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293716 | |||||||
chr1:44293720 | C | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.759-8813G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293720 | |||||||
chr1:44293792 | CCTCA | C | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG02027.hp1 NA18953.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.759-8889_759-8886d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44293792 | |||||||
chr1:44294027 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
228 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.759-9120G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294027 | |||||||
chr1:44294179 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.759-9272A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294179 | |||||||
chr1:44294296 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759-9389T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294296 | |||||||
chr1:44294334 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.759-9427A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294334 | |||||||
chr1:44294364 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759-9457G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294364 | |||||||
chr1:44294431 | C | T | 24 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0148 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.759-9524G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294431 | |||||||
chr1:44294544 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-9637G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294544 | |||||||
chr1:44294558 | T | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-9651A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294558 | |||||||
chr1:44294763 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.759-9856A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44294763 | |||||||
chr1:44295157 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-10250C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44295157 | |||||||
chr1:44295878 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(100): Show |
105 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.759-10971T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44295878 | |||||||
chr1:44296039 | G | A | 26 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(23): Show |
26 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.759-11132C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296039 | |||||||
chr1:44296050 | C | A | 1 | a0001c0001t0001g0036 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.759-11143G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296050 | |||||||
chr1:44296137 | C | A | 3 | a0001c0001t0001g0331 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG01261.hp2 NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.759-11230G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296137 | |||||||
chr1:44296138 | C | G | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | NA18970.hp1 NA18997.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.759-11231G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296138 | |||||||
chr1:44296251 | AG | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0188 a0001c0001t0001g0195 others(4): Show |
7 | HG00621.hp1 HG02738.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.759-11345delC | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296251 | |||||||
chr1:44296306 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.759-11399G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296306 | |||||||
chr1:44296486 | T | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.759-11579A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296486 | |||||||
chr1:44296712 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+11598A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296712 | |||||||
chr1:44296835 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.758+11475G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296835 | |||||||
chr1:44296878 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01243.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.758+11432A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44296878 | |||||||
chr1:44297093 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.758+11217G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297093 | |||||||
chr1:44297120 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0297 a0001c0001t0001g0298 |
3 | HG02559.hp1 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.758+11190G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297120 | |||||||
chr1:44297130 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.758+11180A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297130 | |||||||
chr1:44297682 | A | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.758+10628T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297682 | |||||||
chr1:44297761 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.758+10549A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297761 | |||||||
chr1:44297993 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
227 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.758+10317C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44297993 | |||||||
chr1:44298592 | A | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.758+9718T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298592 | |||||||
chr1:44298631 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(5): Show |
8 | NA18939.hp1 NA18941.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.758+9679G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298631 | |||||||
chr1:44298713 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+9597C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298713 | |||||||
chr1:44298717 | C | A | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.758+9593G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298717 | |||||||
chr1:44298778 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.758+9532G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298778 | |||||||
chr1:44298875 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.758+9435A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298875 | |||||||
chr1:44298946 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.758+9364G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44298946 | |||||||
chr1:44299005 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.758+9305G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299005 | |||||||
chr1:44299180 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.758+9130A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299180 | |||||||
chr1:44299239 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.758+9071C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299239 | |||||||
chr1:44299349 | TTTTTTA | T | 5 | a0001c0001t0001g0115 a0001c0001t0001g0331 a0001c0001t0001g0332 others(2): Show |
5 | HG01261.hp2 HG02293.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+8955_758+8960d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299349 | |||||||
chr1:44299398 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.758+8912T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299398 | |||||||
chr1:44299942 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.758+8368G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299942 | |||||||
chr1:44299974 | C | T | 9 | a0001c0001t0001g0222 a0001c0001t0001g0230 a0001c0001t0001g0238 others(6): Show |
9 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.758+8336G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44299974 | |||||||
chr1:44300182 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.758+8128C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300182 | |||||||
chr1:44300208 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.758+8102C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300208 | |||||||
chr1:44300359 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.758+7951C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300359 | |||||||
chr1:44300399 | C | T | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.758+7911G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300399 | |||||||
chr1:44300419 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.758+7891C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300419 | |||||||
chr1:44300496 | G | C | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.758+7814C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300496 | |||||||
chr1:44300637 | T | G | 6 | a0001c0001t0001g0131 a0001c0001t0001g0148 a0001c0001t0001g0152 others(3): Show |
6 | HG01071.hp1 HG01361.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+7673A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300637 | |||||||
chr1:44300659 | T | A | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.758+7651A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300659 | |||||||
chr1:44300725 | C | T | 27 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(24): Show |
27 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.758+7585G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300725 | |||||||
chr1:44300943 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.758+7367C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44300943 | |||||||
chr1:44301024 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.758+7286C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301024 | |||||||
chr1:44301042 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+7268A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301042 | |||||||
chr1:44301263 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(91): Show |
95 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.758+7047G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301263 | |||||||
chr1:44301299 | C | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.758+7011G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301299 | |||||||
chr1:44301417 | A | C | 1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.758+6893T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301417 | |||||||
chr1:44301506 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.758+6804G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301506 | |||||||
chr1:44301507 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.758+6803A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301507 | |||||||
chr1:44301693 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+6617C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301693 | |||||||
chr1:44301760 | T | C | 28 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.758+6550A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301760 | |||||||
chr1:44301776 | T | C | 10 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(7): Show |
11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.758+6534A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301776 | |||||||
chr1:44301802 | C | T | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0272 others(4): Show |
7 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.758+6508G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301802 | |||||||
chr1:44301868 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.758+6442G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44301868 | |||||||
chr1:44302023 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+6287A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302023 | |||||||
chr1:44302078 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.758+6232T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302078 | |||||||
chr1:44302180 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.758+6130C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302180 | |||||||
chr1:44302241 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.758+6069A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302241 | |||||||
chr1:44302312 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.758+5998T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302312 | |||||||
chr1:44302341 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.758+5969C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302341 | |||||||
chr1:44302467 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.758+5843C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302467 | |||||||
chr1:44302577 | T | G | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.758+5733A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302577 | |||||||
chr1:44302637 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.758+5673A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302637 | |||||||
chr1:44302720 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.758+5590A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302720 | |||||||
chr1:44302725 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.758+5585G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302725 | |||||||
chr1:44302771 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+5539G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302771 | |||||||
chr1:44302965 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.758+5345T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44302965 | |||||||
chr1:44303273 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.758+5037A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303273 | |||||||
chr1:44303451 | G | T | 6 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0256 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.758+4859C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303451 | |||||||
chr1:44303550 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.758+4760A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303550 | |||||||
chr1:44303691 | A | T | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.758+4619T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303691 | |||||||
chr1:44303743 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+4567T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303743 | |||||||
chr1:44303935 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.758+4375A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44303935 | |||||||
chr1:44304140 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.758+4170C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304140 | |||||||
chr1:44304147 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.758+4163A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304147 | |||||||
chr1:44304302 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.758+4008A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304302 | |||||||
chr1:44304357 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.758+3953G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304357 | |||||||
chr1:44304357 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.758+3953G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304357 | |||||||
chr1:44304545 | C | T | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.758+3765G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304545 | |||||||
chr1:44304598 | A | AC | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+3711dupG | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304598 | |||||||
chr1:44304807 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.758+3503T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304807 | |||||||
chr1:44304859 | G | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | NA18959.hp1 NA18970.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+3451C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304859 | |||||||
chr1:44304900 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.758+3410A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44304900 | |||||||
chr1:44305419 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.758+2891C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305419 | |||||||
chr1:44305708 | TATC | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+2599_758+2601d others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305708 | |||||||
chr1:44305802 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+2508C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305802 | |||||||
chr1:44305813 | T | C | 26 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.758+2497A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305813 | |||||||
chr1:44305982 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.758+2328G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44305982 | |||||||
chr1:44306163 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.758+2147G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306163 | |||||||
chr1:44306226 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.758+2084A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306226 | |||||||
chr1:44306409 | C | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
335 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.758+1901G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306409 | |||||||
chr1:44306421 | G | A | 18 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
18 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.758+1889C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306421 | |||||||
chr1:44306421 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.758+1889C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306421 | |||||||
chr1:44306428 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0261 |
3 | HG01167.hp2 HG01169.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.758+1882C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306428 | |||||||
chr1:44306662 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.758+1648G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306662 | |||||||
chr1:44306697 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.758+1613G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306697 | |||||||
chr1:44306730 | C | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
335 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.758+1580G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306730 | |||||||
chr1:44306867 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.758+1443C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306867 | |||||||
chr1:44306954 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
205 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.758+1356A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44306954 | |||||||
chr1:44307059 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+1251T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307059 | |||||||
chr1:44307087 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+1223A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307087 | |||||||
chr1:44307211 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.758+1099A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307211 | |||||||
chr1:44307384 | C | A | 2 | a0001c0001t0001g0301 a0001c0004t0001g0257 |
2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.758+926G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307384 | |||||||
chr1:44307543 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.758+767G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307543 | |||||||
chr1:44307554 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.758+756C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307554 | |||||||
chr1:44307696 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.758+614C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307696 | |||||||
chr1:44307853 | C | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
335 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.758+457G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307853 | |||||||
chr1:44307963 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.758+347A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44307963 | |||||||
chr1:44308055 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
198 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.758+255C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44308055 | |||||||
chr1:44308167 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.758+143G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 6/8 | chr1 | 44308167 | |||||||
chr1:44308511 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.667-110A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308511 | |||||||
chr1:44308615 | T | C | 28 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.667-214A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308615 | |||||||
chr1:44308624 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.667-223C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308624 | |||||||
chr1:44308667 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-266T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308667 | |||||||
chr1:44308955 | G | A | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.667-554C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44308955 | |||||||
chr1:44309340 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.667-939G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309340 | |||||||
chr1:44309701 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.667-1300T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309701 | |||||||
chr1:44309810 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0261 |
3 | HG01167.hp2 HG01169.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.667-1409C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309810 | |||||||
chr1:44309881 | G | A | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.667-1480C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309881 | |||||||
chr1:44309936 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.667-1535G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309936 | |||||||
chr1:44309984 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-1583C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309984 | |||||||
chr1:44309989 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1588C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44309989 | |||||||
chr1:44310043 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.667-1642A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310043 | |||||||
chr1:44310155 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.667-1754G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310155 | |||||||
chr1:44310192 | AG | A | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.667-1792delC | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310192 | |||||||
chr1:44310323 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.667-1922G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310323 | |||||||
chr1:44310379 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.667-1978G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310379 | |||||||
chr1:44310460 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.667-2059T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310460 | |||||||
chr1:44310510 | T | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.667-2109A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310510 | |||||||
chr1:44310535 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-2134C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310535 | |||||||
chr1:44310536 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.667-2135C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310536 | |||||||
chr1:44310568 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.667-2167G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310568 | |||||||
chr1:44310688 | G | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0111 a0001c0001t0001g0222 others(96): Show |
100 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.667-2287C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310688 | |||||||
chr1:44310771 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.667-2370T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310771 | |||||||
chr1:44310910 | GTCTCTCT others(24): Show |
G | 1 | a0001c0001t0001g0328 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.666+2228_666+2258d others(33): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310910 | |||||||
chr1:44310943 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0160 a0001c0001t0001g0187 others(1): Show |
4 | HG02895.hp2 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+2226A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310943 | |||||||
chr1:44310946 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.666+2223C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310946 | |||||||
chr1:44310951 | T | TCG | 33 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0021 others(30): Show |
33 | HG00423.hp2 HG00544.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.666+2216_666+2217d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCG | 18 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(15): Show |
18 | HG00673.hp1 HG02056.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.666+2214_666+2217d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCG | 6 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG00733.hp2 HG03130.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+2212_666+2217d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCGC others(1): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0036 others(4): Show |
7 | HG00408.hp1 HG00738.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+2210_666+2217d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCGC others(3): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0032 |
2 | NA18951.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.666+2208_666+2217d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCGC others(5): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0070 |
2 | HG01109.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.666+2206_666+2217d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCGC others(7): Show |
1 | a0001c0001t0001g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.666+2217_666+2218i others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCGC others(10): Show |
1 | a0001c0001t0001g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.666+2217_666+2218i others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGCGCGC others(6): Show |
1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.666+2217_666+2218i others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310951 | T | TCGTGCGC others(5): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0204 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.666+2217_666+2218i others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310951 | |||||||
chr1:44310952 | C | A | 18 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
18 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.666+2217G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310952 | |||||||
chr1:44310954 | C | CGCGCGCG others(10): Show |
1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.666+2214_666+2215i others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310954 | |||||||
chr1:44310954 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.666+2215G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310954 | |||||||
chr1:44310957 | G | GCGCTGCG others(10): Show |
1 | a0001c0001t0001g0027 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.666+2211_666+2212i others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310957 | |||||||
chr1:44310958 | C | CA | 9 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0143 others(6): Show |
9 | HG02818.hp2 NA18959.hp1 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+2210_666+2211i others(3): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310958 | |||||||
chr1:44310959 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.666+2210C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310959 | |||||||
chr1:44310959 | GCGCGCAC others(11): Show |
G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
2 | NA18941.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.666+2192_666+2209d others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310959 | |||||||
chr1:44310960 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0160 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.666+2209G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310960 | |||||||
chr1:44310961 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.666+2208C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310961 | |||||||
chr1:44310962 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.666+2207G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310962 | |||||||
chr1:44310962 | C | CGCGCGCG others(4): Show |
1 | a0001c0001t0001g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666+2206_666+2207i others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310962 | |||||||
chr1:44310963 | G | GCGCGCGC others(13): Show |
1 | a0001c0001t0001g0297 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.666+2205_666+2206i others(22): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCA | G | 52 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(49): Show |
52 | HG00558.hp1 HG00673.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.666+2204_666+2205d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACA | G | 42 | a0001c0001t0001g0038 a0001c0001t0001g0060 a0001c0001t0001g0066 others(39): Show |
42 | HG00408.hp2 HG00639.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.666+2202_666+2205d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACA | G | 24 | a0001c0001t0001g0029 a0001c0001t0001g0062 a0001c0001t0001g0073 others(21): Show |
24 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.666+2200_666+2205d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACAC others(1): Show |
G | 20 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0140 others(17): Show |
20 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.666+2198_666+2205d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACAC others(3): Show |
G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG00280.hp2 HG01167.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.666+2196_666+2205d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACAC others(5): Show |
G | 6 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0123 others(3): Show |
6 | HG02717.hp1 HG02965.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+2194_666+2205d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACAC others(7): Show |
G | 7 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG02148.hp1 NA18939.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+2192_666+2205d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACAC others(9): Show |
G | 11 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.666+2190_666+2205d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310963 | GCACACAC others(11): Show |
G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0240 others(7): Show |
11 | HG00733.hp1 HG01175.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.666+2188_666+2205d others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310963 | |||||||
chr1:44310964 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.666+2205G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310964 | |||||||
chr1:44310965 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(145): Show |
149 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.666+2204T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310965 | |||||||
chr1:44310967 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
190 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.666+2202T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310967 | |||||||
chr1:44310967 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.666+2202T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310967 | |||||||
chr1:44310968 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.666+2201G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310968 | |||||||
chr1:44310969 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
224 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.666+2200T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310969 | |||||||
chr1:44310971 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.666+2198T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310971 | |||||||
chr1:44310973 | A | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
155 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.666+2196T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310973 | |||||||
chr1:44310974 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.666+2195G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310974 | |||||||
chr1:44310975 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(91): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.666+2194T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310975 | |||||||
chr1:44310977 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0031 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.666+2192T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310977 | |||||||
chr1:44310979 | A | G | 24 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0066 others(21): Show |
24 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.666+2190T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310979 | |||||||
chr1:44310981 | A | G | 18 | a0001c0001t0001g0051 a0001c0001t0001g0073 a0001c0001t0001g0095 others(15): Show |
18 | HG00438.hp1 HG01261.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.666+2188T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310981 | |||||||
chr1:44310983 | A | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0109 others(4): Show |
7 | HG02818.hp1 HG03209.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+2186T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310983 | |||||||
chr1:44310985 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0109 |
2 | HG02818.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.666+2184T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310985 | |||||||
chr1:44310986 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2183G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310986 | |||||||
chr1:44310987 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0165 |
2 | NA19030.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.666+2182T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310987 | |||||||
chr1:44310989 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2180T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310989 | |||||||
chr1:44310991 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2178T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44310991 | |||||||
chr1:44311015 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666+2154T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311015 | |||||||
chr1:44311016 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666+2153G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311016 | |||||||
chr1:44311017 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.666+2152C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311017 | |||||||
chr1:44311029 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.666+2140T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311029 | |||||||
chr1:44311512 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.666+1657G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311512 | |||||||
chr1:44311918 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.666+1251A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44311918 | |||||||
chr1:44312157 | C | G | 1 | a0001c0001t0001g0016 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.666+1012G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312157 | |||||||
chr1:44312300 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.666+869C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312300 | |||||||
chr1:44312394 | T | C | 1 | a0001c0004t0001g0257 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.666+775A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312394 | |||||||
chr1:44312738 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.666+431G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312738 | |||||||
chr1:44312819 | T | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0159 a0001c0001t0001g0197 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+350A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312819 | |||||||
chr1:44312908 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.666+261A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312908 | |||||||
chr1:44312980 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+189G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 5/8 | chr1 | 44312980 | |||||||
chr1:44313295 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.607-67G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313295 | |||||||
chr1:44313475 | G | A | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-247C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313475 | |||||||
chr1:44313528 | A | C | 6 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0160 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-300T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313528 | |||||||
chr1:44313657 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02717.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.607-429A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313657 | |||||||
chr1:44313814 | C | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0155 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.607-586G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313814 | |||||||
chr1:44313892 | T | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0178 others(2): Show |
5 | HG00280.hp1 HG01081.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-664A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313892 | |||||||
chr1:44313985 | T | TA | 9 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-758dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44313985 | |||||||
chr1:44314075 | C | A | 1 | a0001c0001t0001g0010 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.607-847G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314075 | |||||||
chr1:44314139 | T | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02056.hp2 HG02132.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.607-911A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314139 | |||||||
chr1:44314153 | T | TG | 173 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0042 others(170): Show |
175 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.607-926dupC | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314153 | |||||||
chr1:44314248 | G | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0034 others(2): Show |
6 | HG02040.hp1 HG02080.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-1020C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314248 | |||||||
chr1:44314319 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.607-1091G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314319 | |||||||
chr1:44314339 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.607-1111C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314339 | |||||||
chr1:44314526 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-1298A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314526 | |||||||
chr1:44314559 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.607-1331C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314559 | |||||||
chr1:44314650 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.607-1422G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314650 | |||||||
chr1:44314740 | G | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-1512C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314740 | |||||||
chr1:44314779 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.607-1551G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314779 | |||||||
chr1:44314896 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.607-1668G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314896 | |||||||
chr1:44314901 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.607-1673A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314901 | |||||||
chr1:44314947 | A | C | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-1719T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44314947 | |||||||
chr1:44315123 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.607-1895T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315123 | |||||||
chr1:44315371 | A | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-2143T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315371 | |||||||
chr1:44315480 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-2252G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315480 | |||||||
chr1:44315611 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607-2383A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315611 | |||||||
chr1:44315664 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.607-2436A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315664 | |||||||
chr1:44315811 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.607-2583G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315811 | |||||||
chr1:44315983 | CT | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
291 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.607-2756delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44315983 | |||||||
chr1:44316087 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-2859A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44316087 | |||||||
chr1:44316306 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.607-3078C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44316306 | |||||||
chr1:44316919 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.606+2709G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44316919 | |||||||
chr1:44317000 | T | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
38 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.606+2628A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317000 | |||||||
chr1:44317082 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2546A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317082 | |||||||
chr1:44317117 | G | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+2511C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317117 | |||||||
chr1:44317144 | G | GCA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0127 others(111): Show |
116 | HG00438.hp2 HG00544.hp2 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.606+2482_606+2483d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317144 | G | GCACA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
103 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.606+2480_606+2483d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317144 | G | GCACACA | 16 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0044 others(13): Show |
16 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.606+2478_606+2483d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317144 | G | GCACACAC others(1): Show |
18 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
18 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.606+2476_606+2483d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317144 | G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0060 others(4): Show |
7 | HG01106.hp2 HG01256.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.606+2474_606+2483d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317144 | G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0082 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.606+2472_606+2483d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317144 | GCA | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0001g0325 |
3 | HG02040.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.606+2482_606+2483d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317144 | |||||||
chr1:44317499 | G | GACAGAAA others(22): Show |
4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2100_606+2128d others(31): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317499 | |||||||
chr1:44317585 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0270 a0001c0001t0001g0292 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2043C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317585 | |||||||
chr1:44317649 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.606+1979A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317649 | |||||||
chr1:44317695 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.606+1933G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317695 | |||||||
chr1:44317813 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.606+1815T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44317813 | |||||||
chr1:44318300 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.606+1328C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318300 | |||||||
chr1:44318603 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.606+1025C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318603 | |||||||
chr1:44318620 | C | T | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.606+1008G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318620 | |||||||
chr1:44318699 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+929T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318699 | |||||||
chr1:44318725 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.606+903G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318725 | |||||||
chr1:44318812 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.606+816T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44318812 | |||||||
chr1:44319045 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.606+583A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319045 | |||||||
chr1:44319110 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.606+518G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319110 | |||||||
chr1:44319174 | T | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+454A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319174 | |||||||
chr1:44319199 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.606+429C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319199 | |||||||
chr1:44319325 | C | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.606+303G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 4/8 | chr1 | 44319325 | |||||||
chr1:44319899 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-155C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44319899 | |||||||
chr1:44320014 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.490-270G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320014 | |||||||
chr1:44320159 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490-415T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320159 | |||||||
chr1:44320400 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
335 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.490-656T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320400 | |||||||
chr1:44320502 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.490-758G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320502 | |||||||
chr1:44320519 | G | A | 1 | a0001c0002t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.490-775C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320519 | |||||||
chr1:44320564 | G | A | 5 | a0001c0001t0001g0242 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG00544.hp2 NA18963.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-820C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320564 | |||||||
chr1:44320711 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.490-967G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44320711 | |||||||
chr1:44321061 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.490-1317T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321061 | |||||||
chr1:44321503 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.490-1759A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321503 | |||||||
chr1:44321566 | C | A | 6 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0256 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1822G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321566 | |||||||
chr1:44321608 | A | G | 5 | a0001c0001t0001g0251 a0001c0001t0001g0267 a0001c0001t0001g0283 others(2): Show |
5 | HG00738.hp1 HG01256.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-1864T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321608 | |||||||
chr1:44321660 | C | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0093 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.490-1916G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321660 | |||||||
chr1:44321994 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.490-2250T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44321994 | |||||||
chr1:44322101 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2357G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44322101 | |||||||
chr1:44322306 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.490-2562C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44322306 | |||||||
chr1:44322726 | A | T | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.490-2982T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44322726 | |||||||
chr1:44323243 | T | C | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-3499A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323243 | |||||||
chr1:44323558 | C | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0278 a0001c0001t0001g0310 |
3 | NA18952.hp2 NA19004.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.490-3814G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323558 | |||||||
chr1:44323583 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-3839A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323583 | |||||||
chr1:44323593 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-3849C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44323593 | |||||||
chr1:44324050 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.490-4306C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324050 | |||||||
chr1:44324221 | A | C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4477T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324221 | |||||||
chr1:44324394 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.490-4650A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324394 | |||||||
chr1:44324433 | CTGTT | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0090 |
4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4693_490-4690d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324433 | |||||||
chr1:44324455 | G | C | 27 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(24): Show |
27 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-4711C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324455 | |||||||
chr1:44324476 | C | CT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
184 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.490-4733dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324476 | |||||||
chr1:44324476 | C | CTT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0033 others(16): Show |
19 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-4734_490-4733d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324476 | |||||||
chr1:44324630 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4886G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324630 | |||||||
chr1:44324718 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.490-4974C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324718 | |||||||
chr1:44324851 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490-5107T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324851 | |||||||
chr1:44324870 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02056.hp2 HG02132.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.490-5126G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324870 | |||||||
chr1:44324894 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490-5150T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324894 | |||||||
chr1:44324981 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(101): Show |
106 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.490-5237A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44324981 | |||||||
chr1:44325057 | C | A | 1 | a0001c0001t0001g0331 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.490-5313G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325057 | |||||||
chr1:44325075 | CT | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
197 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.490-5332delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325075 | |||||||
chr1:44325075 | CTT | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0001g0228 others(96): Show |
101 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.490-5333_490-5332d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325075 | |||||||
chr1:44325156 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.490-5412A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325156 | |||||||
chr1:44325163 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5419G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325163 | |||||||
chr1:44325327 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.490-5583C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325327 | |||||||
chr1:44325354 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-5610G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325354 | |||||||
chr1:44325522 | T | C | 24 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0148 others(21): Show |
24 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-5778A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325522 | |||||||
chr1:44325561 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5817T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325561 | |||||||
chr1:44325850 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-6106G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44325850 | |||||||
chr1:44326175 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0241 others(3): Show |
7 | NA18966.hp2 NA19012.hp2 NA19058.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-6431C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326175 | |||||||
chr1:44326274 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490-6530T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326274 | |||||||
chr1:44326345 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-6601A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326345 | |||||||
chr1:44326464 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.490-6720G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326464 | |||||||
chr1:44326653 | T | C | 1 | a0001c0001t0001g0003 | 2 | NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.490-6909A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326653 | |||||||
chr1:44326841 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.490-7097G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326841 | |||||||
chr1:44326996 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.490-7252G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44326996 | |||||||
chr1:44327009 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.490-7265A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327009 | |||||||
chr1:44327666 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0288 |
2 | NA18982.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.490-7922G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327666 | |||||||
chr1:44327746 | T | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-8002A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327746 | |||||||
chr1:44327779 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0090 |
4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-8035T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327779 | |||||||
chr1:44327981 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.490-8237G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327981 | |||||||
chr1:44327985 | G | C | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-8241C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327985 | |||||||
chr1:44327995 | A | G | 72 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0117 others(69): Show |
72 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.490-8251T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44327995 | |||||||
chr1:44328088 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
96 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.490-8344C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328088 | |||||||
chr1:44328234 | C | T | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0299 others(1): Show |
4 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-8490G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328234 | |||||||
chr1:44328248 | C | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0241 others(3): Show |
7 | NA18966.hp2 NA19012.hp2 NA19058.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-8504G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328248 | |||||||
chr1:44328409 | T | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
336 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.490-8665A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44328409 | |||||||
chr1:44329134 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-9390G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329134 | |||||||
chr1:44329253 | C | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-9509G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329253 | |||||||
chr1:44329600 | A | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0266 |
2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.489+9445T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329600 | |||||||
chr1:44329789 | G | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+9256C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44329789 | |||||||
chr1:44330124 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.489+8921G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44330124 | |||||||
chr1:44331130 | C | G | 29 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(26): Show |
29 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+7915G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331130 | |||||||
chr1:44331262 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489+7783A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331262 | |||||||
chr1:44331270 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
335 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.489+7775T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331270 | |||||||
chr1:44331301 | AT | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0078 others(6): Show |
9 | HG01169.hp2 HG02735.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+7743delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331301 | |||||||
chr1:44331328 | A | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+7717T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331328 | |||||||
chr1:44331474 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+7571A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331474 | |||||||
chr1:44331573 | C | G | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.489+7472G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331573 | |||||||
chr1:44331719 | A | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+7326T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331719 | |||||||
chr1:44331794 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.489+7251T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331794 | |||||||
chr1:44331808 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+7237A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331808 | |||||||
chr1:44331836 | G | T | 10 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(7): Show |
10 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+7209C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331836 | |||||||
chr1:44331867 | T | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0183 |
2 | HG00423.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.489+7178A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44331867 | |||||||
chr1:44332258 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+6787A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332258 | |||||||
chr1:44332332 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+6713G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332332 | |||||||
chr1:44332372 | G | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0299 others(1): Show |
4 | HG01081.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6673C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332372 | |||||||
chr1:44332451 | C | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(3): Show |
6 | NA18939.hp1 NA18941.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+6594G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332451 | |||||||
chr1:44332519 | A | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0034 others(1): Show |
5 | HG02080.hp2 NA18954.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+6526T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332519 | |||||||
chr1:44332669 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0161 a0001c0001t0001g0165 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6376G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332669 | |||||||
chr1:44332700 | G | A | 71 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.489+6345C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332700 | |||||||
chr1:44332703 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6342T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332703 | |||||||
chr1:44332863 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+6182A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332863 | |||||||
chr1:44332867 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.489+6178C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332867 | |||||||
chr1:44332978 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.489+6067C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44332978 | |||||||
chr1:44333067 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.489+5978A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333067 | |||||||
chr1:44333110 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.489+5935A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333110 | |||||||
chr1:44333113 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.489+5932A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333113 | |||||||
chr1:44333319 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0001g0295 a0001c0001t0001g0296 |
3 | HG02258.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.489+5726C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333319 | |||||||
chr1:44333325 | G | A | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+5720C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333325 | |||||||
chr1:44333362 | C | A | 28 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.489+5683G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333362 | |||||||
chr1:44333406 | C | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+5639G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333406 | |||||||
chr1:44333452 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.489+5593T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333452 | |||||||
chr1:44333505 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.489+5540G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333505 | |||||||
chr1:44333630 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0205 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+5415G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333630 | |||||||
chr1:44333711 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.489+5334G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333711 | |||||||
chr1:44333872 | C | T | 11 | a0001c0001t0001g0111 a0001c0001t0001g0233 a0001c0001t0001g0234 others(8): Show |
11 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+5173G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333872 | |||||||
chr1:44333927 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+5118C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44333927 | |||||||
chr1:44334018 | G | T | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+5027C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334018 | |||||||
chr1:44334023 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.489+5022G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334023 | |||||||
chr1:44334129 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489+4916G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334129 | |||||||
chr1:44334280 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0085 others(1): Show |
4 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+4765A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334280 | |||||||
chr1:44334333 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.489+4712T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334333 | |||||||
chr1:44334588 | A | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+4457T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334588 | |||||||
chr1:44334708 | C | G | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+4337G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334708 | |||||||
chr1:44334826 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0044 others(16): Show |
19 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.489+4219C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334826 | |||||||
chr1:44334868 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.489+4177A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334868 | |||||||
chr1:44334878 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+4167T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44334878 | |||||||
chr1:44335116 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.489+3929A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335116 | |||||||
chr1:44335168 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0231 |
3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.489+3877G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335168 | |||||||
chr1:44335219 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.489+3826G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335219 | |||||||
chr1:44335313 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489+3732T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335313 | |||||||
chr1:44335320 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3725T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335320 | |||||||
chr1:44335354 | C | CA | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+3690dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335354 | |||||||
chr1:44335425 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+3620T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335425 | |||||||
chr1:44335489 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+3556C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335489 | |||||||
chr1:44335499 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.489+3546G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335499 | |||||||
chr1:44335502 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
228 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.489+3543C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335502 | |||||||
chr1:44335547 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+3498C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335547 | |||||||
chr1:44335576 | A | G | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.489+3469T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335576 | |||||||
chr1:44335588 | G | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(331): Show |
337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.489+3457C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335588 | |||||||
chr1:44335699 | C | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3346G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335699 | |||||||
chr1:44335776 | C | CA | 15 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0137 others(12): Show |
15 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+3268dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335776 | |||||||
chr1:44335992 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.489+3053A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44335992 | |||||||
chr1:44336017 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.489+3028A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336017 | |||||||
chr1:44336396 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2649C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336396 | |||||||
chr1:44336553 | TA | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.489+2491delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336553 | |||||||
chr1:44336977 | T | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.489+2068A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44336977 | |||||||
chr1:44337565 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+1480G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337565 | |||||||
chr1:44337674 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0111 a0001c0001t0001g0228 others(95): Show |
99 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.489+1371A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337674 | |||||||
chr1:44337799 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.489+1246A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337799 | |||||||
chr1:44337831 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
6 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+1214C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337831 | |||||||
chr1:44337840 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+1205C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337840 | |||||||
chr1:44337843 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.489+1202C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44337843 | |||||||
chr1:44338241 | T | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+804A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338241 | |||||||
chr1:44338344 | C | T | 18 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0167 others(15): Show |
18 | HG01884.hp1 HG01943.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+701G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338344 | |||||||
chr1:44338457 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0310 |
2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.489+588A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338457 | |||||||
chr1:44338489 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.489+556T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338489 | |||||||
chr1:44338586 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+459C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338586 | |||||||
chr1:44338686 | A | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.489+359T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338686 | |||||||
chr1:44338808 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+237C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338808 | |||||||
chr1:44338961 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.489+84G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 3/8 | chr1 | 44338961 | |||||||
chr1:44339340 | TA | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0046 others(19): Show |
23 | HG01167.hp1 HG01169.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.212-19delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339340 | |||||||
chr1:44339341 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.212-19T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339341 | |||||||
chr1:44339354 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.212-32T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339354 | |||||||
chr1:44339689 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-367G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44339689 | |||||||
chr1:44340023 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-701A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340023 | |||||||
chr1:44340034 | TCGA | T | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-715_212-713del others(3): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340034 | |||||||
chr1:44340145 | T | G | 4 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-823A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340145 | |||||||
chr1:44340149 | CA | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
320 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.212-828delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44340149 | |||||||
chr1:44341064 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-1742G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341064 | |||||||
chr1:44341466 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.212-2144A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341466 | |||||||
chr1:44341492 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
199 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.212-2170G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341492 | |||||||
chr1:44341497 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-2175C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341497 | |||||||
chr1:44341542 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
231 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.212-2220A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341542 | |||||||
chr1:44341718 | C | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18970.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.212-2396G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341718 | |||||||
chr1:44341890 | AAAAAC | A | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.212-2573_212-2569d others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341890 | |||||||
chr1:44341938 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.212-2616C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341938 | |||||||
chr1:44341990 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.212-2668C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44341990 | |||||||
chr1:44342113 | C | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0240 others(11): Show |
15 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-2791G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342113 | |||||||
chr1:44342121 | T | C | 69 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.212-2799A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342121 | |||||||
chr1:44342515 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3193C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342515 | |||||||
chr1:44342519 | C | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3197G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342519 | |||||||
chr1:44342535 | T | TAC | 28 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0125 others(25): Show |
28 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.212-3215_212-3214d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342535 | |||||||
chr1:44342643 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.212-3321A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342643 | |||||||
chr1:44342646 | C | T | 29 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(26): Show |
29 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-3324G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342646 | |||||||
chr1:44342653 | G | GT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0240 others(11): Show |
15 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-3332dupA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342653 | |||||||
chr1:44342789 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.212-3467C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342789 | |||||||
chr1:44342811 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
230 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.212-3489A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342811 | |||||||
chr1:44342812 | A | AATAT | 3 | a0001c0001t0001g0025 a0001c0001t0001g0287 a0001c0001t0001g0299 |
3 | HG01361.hp1 NA18939.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.212-3494_212-3491d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342812 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0285 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.212-3500_212-3491d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342812 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0062 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.212-3504_212-3491d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342812 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0286 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.212-3506_212-3491d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342812 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.212-3490T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342812 | AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0307 |
2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-3502_212-3491d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342812 | AATATATA others(19): Show |
A | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.212-3516_212-3491d others(28): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342812 | |||||||
chr1:44342813 | A | C | 1 | a0001c0001t0001g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.212-3491T>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342813 | |||||||
chr1:44342814 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-3492A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342814 | |||||||
chr1:44342820 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0134 a0001c0003t0001g0219 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.212-3499_212-3498i others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342820 | |||||||
chr1:44342820 | T | TATATATA others(32): Show |
1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.212-3499_212-3498i others(41): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342820 | |||||||
chr1:44342821 | ATATATAT others(33): Show |
A | 1 | a0001c0001t0001g0320 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.212-3539_212-3500d others(42): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342821 | |||||||
chr1:44342822 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.212-3501_212-3500i others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342822 | |||||||
chr1:44342824 | T | TATATATA others(3): Show |
2 | a0001c0001t0001g0178 a0001c0001t0001g0223 |
2 | HG01358.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.212-3503_212-3502i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342824 | |||||||
chr1:44342824 | T | TATATATA others(15): Show |
1 | a0001c0001t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.212-3503_212-3502i others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342824 | |||||||
chr1:44342826 | T | TATATATA others(33): Show |
1 | a0001c0001t0001g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.212-3505_212-3504i others(42): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342826 | |||||||
chr1:44342827 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.212-3536_212-3506d others(33): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342827 | |||||||
chr1:44342827 | ATATATAT others(25): Show |
A | 16 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(13): Show |
16 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-3537_212-3506d others(34): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342827 | |||||||
chr1:44342828 | T | TATATAA | 13 | a0001c0001t0001g0131 a0001c0001t0001g0148 a0001c0001t0001g0150 others(10): Show |
13 | HG01106.hp1 HG01361.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-3507_212-3506i others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342828 | |||||||
chr1:44342828 | T | TATATAAA others(33): Show |
1 | a0001c0001t0001g0185 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.212-3507_212-3506i others(42): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342828 | |||||||
chr1:44342829 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.212-3537_212-3508d others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342829 | |||||||
chr1:44342829 | ATATATAT others(25): Show |
A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0119 |
2 | HG02293.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.212-3539_212-3508d others(34): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342829 | |||||||
chr1:44342829 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0013 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.212-3545_212-3508d others(40): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342829 | |||||||
chr1:44342830 | TATATATA others(20): Show |
T | 1 | a0001c0001t0001g0331 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.212-3535_212-3509d others(29): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342830 | |||||||
chr1:44342831 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.212-3546_212-3510d others(39): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342831 | |||||||
chr1:44342833 | ATATATAT others(21): Show |
A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0231 |
3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.212-3539_212-3512d others(30): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342833 | |||||||
chr1:44342834 | T | A | 27 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(24): Show |
27 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-3512A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342834 | |||||||
chr1:44342835 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-3540_212-3514d others(29): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342835 | |||||||
chr1:44342835 | ATATATAT others(28): Show |
A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0226 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.212-3548_212-3514d others(37): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342835 | |||||||
chr1:44342836 | T | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG02922.hp2 NA18949.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-3514A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342836 | |||||||
chr1:44342836 | TATATATA others(14): Show |
T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0332 |
2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.212-3535_212-3515d others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342836 | |||||||
chr1:44342837 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0253 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.212-3538_212-3516d others(25): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342837 | |||||||
chr1:44342837 | ATATATAT others(23): Show |
A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG01943.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-3545_212-3516d others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342837 | |||||||
chr1:44342837 | ATATATAT others(28): Show |
A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | HG01243.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.212-3550_212-3516d others(37): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342837 | |||||||
chr1:44342838 | T | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0160 others(2): Show |
5 | HG02723.hp2 HG02895.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-3516A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342838 | |||||||
chr1:44342839 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.212-3538_212-3518d others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | |||||||
chr1:44342839 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0250 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.212-3539_212-3518d others(24): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | |||||||
chr1:44342839 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.212-3544_212-3518d others(29): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | |||||||
chr1:44342839 | ATATATAT others(23): Show |
A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0209 |
2 | HG02056.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-3547_212-3518d others(32): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342839 | |||||||
chr1:44342841 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212-3545_212-3520d others(28): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342841 | |||||||
chr1:44342841 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.212-3548_212-3520d others(31): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342841 | |||||||
chr1:44342841 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-3551_212-3520d others(34): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342841 | |||||||
chr1:44342843 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.212-3542_212-3522d others(23): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342843 | |||||||
chr1:44342844 | T | A | 1 | a0001c0001t0005g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212-3522A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342844 | |||||||
chr1:44342845 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0033 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.212-3539_212-3524d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342845 | |||||||
chr1:44342845 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.212-3547_212-3524d others(26): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342845 | |||||||
chr1:44342847 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.212-3538_212-3526d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342847 | |||||||
chr1:44342847 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0292 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.212-3542_212-3526d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342847 | |||||||
chr1:44342848 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.212-3526A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342848 | |||||||
chr1:44342849 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0266 |
2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.212-3537_212-3528d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | |||||||
chr1:44342849 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.212-3540_212-3528d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | |||||||
chr1:44342849 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.212-3541_212-3528d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | |||||||
chr1:44342849 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0293 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212-3544_212-3528d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | |||||||
chr1:44342849 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0030 |
2 | NA18995.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.212-3545_212-3528d others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | |||||||
chr1:44342849 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.212-3546_212-3528d others(21): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342849 | |||||||
chr1:44342850 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.212-3528A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342850 | |||||||
chr1:44342851 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0317 |
2 | HG00438.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.212-3539_212-3530d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | |||||||
chr1:44342851 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.212-3540_212-3530d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | |||||||
chr1:44342851 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.212-3542_212-3530d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | |||||||
chr1:44342851 | ATATATAT others(7): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0090 |
4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3543_212-3530d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | |||||||
chr1:44342851 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.212-3544_212-3530d others(17): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | |||||||
chr1:44342851 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.212-3546_212-3530d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342851 | |||||||
chr1:44342853 | ATATATTT others(3): Show |
A | 7 | a0001c0001t0001g0244 a0001c0001t0001g0248 a0001c0001t0001g0265 others(4): Show |
7 | HG03017.hp2 HG04204.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-3541_212-3532d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342853 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.212-3542_212-3532d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342853 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.212-3543_212-3532d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342853 | ATATATTT others(6): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.212-3544_212-3532d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342853 | ATATATTT others(7): Show |
A | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.212-3545_212-3532d others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342853 | ATATATTT others(8): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.212-3546_212-3532d others(17): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342853 | ATATATTT others(10): Show |
A | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-3548_212-3532d others(19): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342853 | |||||||
chr1:44342855 | ATATTTTT others(3): Show |
A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0170 a0001c0001t0001g0314 |
3 | HG01884.hp1 NA18945.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.212-3543_212-3534d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | |||||||
chr1:44342855 | ATATTTTT others(4): Show |
A | 1 | a0001c0001t0001g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.212-3544_212-3534d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | |||||||
chr1:44342855 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0006 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.212-3545_212-3534d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | |||||||
chr1:44342855 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0319 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.212-3546_212-3534d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342855 | |||||||
chr1:44342857 | A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0143 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.212-3536_212-3535i others(45): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | ATATATAT others(70): Show |
1 | a0001c0001t0001g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(79): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0295 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0197 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-3536_212-3535i others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.212-3536_212-3535i others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | A | T | 6 | a0001c0001t0001g0134 a0001c0001t0001g0188 a0001c0001t0001g0305 others(3): Show |
6 | HG00733.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3535T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | AT | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0087 others(5): Show |
8 | HG01257.hp1 HG01496.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-3536delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATT | A | 14 | a0001c0001t0001g0027 a0001c0001t0001g0127 a0001c0001t0001g0200 others(11): Show |
14 | HG00544.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-3537_212-3536d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTT | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0073 others(3): Show |
6 | HG02630.hp1 HG03654.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3538_212-3536d others(5): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTT | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0034 others(3): Show |
6 | HG01516.hp1 HG02080.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3539_212-3536d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTT | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0048 others(7): Show |
10 | HG00642.hp1 HG00673.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-3540_212-3536d others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTT | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(20): Show |
23 | HG00408.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-3541_212-3536d others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0039 others(8): Show |
11 | HG01516.hp2 HG02148.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-3542_212-3536d others(9): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT others(1): Show |
A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.212-3543_212-3536d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT others(2): Show |
A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0061 others(5): Show |
8 | HG00544.hp1 HG00733.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-3544_212-3536d others(11): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT others(3): Show |
A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0031 others(8): Show |
11 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.212-3545_212-3536d others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.212-3546_212-3536d others(13): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.212-3548_212-3536d others(15): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342857 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.212-3551_212-3536d others(18): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342857 | |||||||
chr1:44342858 | T | TA | 4 | a0001c0001t0001g0116 a0001c0001t0001g0158 a0001c0001t0001g0199 others(1): Show |
4 | HG01243.hp1 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3537_212-3536i others(3): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATA | 6 | a0001c0001t0001g0059 a0001c0001t0001g0126 a0001c0001t0001g0149 others(3): Show |
6 | HG02738.hp2 HG02895.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-3537_212-3536i others(7): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATAAA others(30): Show |
3 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0221 |
3 | HG00280.hp1 HG01433.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(39): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(25): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(32): Show |
1 | a0001c0001t0001g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(41): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(34): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0140 |
2 | NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(43): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(58): Show |
1 | a0001c0001t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(67): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(62): Show |
1 | a0001c0001t0001g0144 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(71): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(34): Show |
1 | a0001c0001t0001g0177 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(43): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(36): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0184 |
2 | NA18949.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(45): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(36): Show |
1 | a0001c0001t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(45): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(38): Show |
1 | a0001c0001t0001g0129 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(47): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(40): Show |
1 | a0001c0001t0001g0138 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(49): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(42): Show |
1 | a0001c0001t0001g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(51): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(42): Show |
1 | a0001c0001t0001g0181 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(51): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(42): Show |
1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.212-3537_212-3536i others(51): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(12): Show |
1 | a0001c0001t0005g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.212-3537_212-3536i others(21): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342858 | T | TATATATA others(18): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.212-3537_212-3536i others(27): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342858 | |||||||
chr1:44342859 | T | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0045 others(24): Show |
27 | HG00408.hp2 HG01106.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-3537A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342859 | |||||||
chr1:44342860 | T | A | 28 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0059 others(25): Show |
28 | HG00423.hp1 HG00558.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.212-3538A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342860 | |||||||
chr1:44342861 | T | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0027 others(21): Show |
24 | HG00544.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.212-3539A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342861 | |||||||
chr1:44342862 | T | A | 18 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0049 others(15): Show |
18 | HG01257.hp1 HG01496.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-3540A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342862 | |||||||
chr1:44342863 | T | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(18): Show |
21 | HG01175.hp1 HG01256.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.212-3541A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342863 | |||||||
chr1:44342864 | T | A | 22 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0040 others(19): Show |
22 | HG00642.hp1 HG00673.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.212-3542A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342864 | |||||||
chr1:44342865 | T | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(24): Show |
27 | HG00408.hp1 HG01071.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-3543A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342865 | |||||||
chr1:44342866 | T | A | 23 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0039 others(20): Show |
23 | HG00642.hp1 HG00673.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-3544A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342866 | |||||||
chr1:44342867 | T | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
34 | HG00408.hp1 HG00639.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-3545A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342867 | |||||||
chr1:44342868 | T | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0047 others(10): Show |
13 | HG00544.hp1 HG00733.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-3546A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342868 | |||||||
chr1:44342869 | T | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
13 | HG00408.hp1 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.212-3547A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342869 | |||||||
chr1:44342870 | T | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG01496.hp2 NA18968.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3548A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342870 | |||||||
chr1:44342871 | T | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0200 others(1): Show |
4 | HG01175.hp1 HG02040.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-3549A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342871 | |||||||
chr1:44342872 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.212-3550A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44342872 | |||||||
chr1:44343115 | T | A | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.212-3793A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343115 | |||||||
chr1:44343236 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-3914G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343236 | |||||||
chr1:44343397 | G | A | 22 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(19): Show |
22 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.212-4075C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343397 | |||||||
chr1:44343556 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.212-4234G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343556 | |||||||
chr1:44343766 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.212-4444A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343766 | |||||||
chr1:44343773 | T | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(255): Show |
261 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.212-4451A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343773 | |||||||
chr1:44343986 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-4664G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44343986 | |||||||
chr1:44344045 | C | T | 25 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0129 others(22): Show |
25 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.212-4723G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344045 | |||||||
chr1:44344233 | C | CAATA | 42 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0129 others(39): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.212-4915_212-4912d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | |||||||
chr1:44344233 | C | CAATAAAT others(1): Show |
8 | a0001c0001t0001g0134 a0001c0001t0001g0159 a0001c0001t0001g0185 others(5): Show |
8 | HG01081.hp2 HG01257.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-4919_212-4912d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | |||||||
chr1:44344233 | CAATA | C | 99 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0055 others(96): Show |
99 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.212-4915_212-4912d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | |||||||
chr1:44344233 | CAATAAAT others(1): Show |
C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
86 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.212-4919_212-4912d others(10): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | |||||||
chr1:44344233 | CAATAAAT others(5): Show |
C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0203 a0001c0001t0001g0204 others(2): Show |
6 | HG01884.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-4923_212-4912d others(14): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | |||||||
chr1:44344233 | CAATAAAT others(13): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.212-4931_212-4912d others(22): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344233 | |||||||
chr1:44344276 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.212-4954A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344276 | |||||||
chr1:44344506 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.212-5184C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344506 | |||||||
chr1:44344740 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.212-5418G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344740 | |||||||
chr1:44344932 | G | C | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.212-5610C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344932 | |||||||
chr1:44344946 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.212-5624G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44344946 | |||||||
chr1:44345001 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.212-5679T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345001 | |||||||
chr1:44345383 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.212-6061G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345383 | |||||||
chr1:44345741 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.212-6419G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345741 | |||||||
chr1:44345902 | C | T | 1 | a0001c0001t0001g0003 | 2 | NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.212-6580G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44345902 | |||||||
chr1:44346138 | C | T | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+6712G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346138 | |||||||
chr1:44346173 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+6677C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346173 | |||||||
chr1:44346519 | C | A | 20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00280.hp2 HG01261.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+6331G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346519 | |||||||
chr1:44346966 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+5884A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44346966 | |||||||
chr1:44347320 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.211+5530T>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347320 | |||||||
chr1:44347409 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.211+5441A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347409 | |||||||
chr1:44347575 | C | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+5275G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347575 | |||||||
chr1:44347775 | T | TA | 24 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(21): Show |
24 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.211+5074dupT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347775 | |||||||
chr1:44347775 | TA | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
232 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.211+5074delT | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347775 | |||||||
chr1:44347792 | T | C | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+5058A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347792 | |||||||
chr1:44347879 | T | TTG | 64 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(61): Show |
64 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.211+4969_211+4970d others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347879 | |||||||
chr1:44347879 | T | TTGTG | 7 | a0001c0001t0001g0003 a0001c0001t0001g0098 a0001c0001t0001g0224 others(4): Show |
8 | HG00639.hp2 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.211+4967_211+4970d others(6): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347879 | |||||||
chr1:44347941 | A | G | 28 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(25): Show |
28 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.211+4909T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44347941 | |||||||
chr1:44348261 | C | A | 5 | a0001c0001t0001g0242 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG00544.hp2 NA18963.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+4589G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348261 | |||||||
chr1:44348710 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG02630.hp2 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+4140T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348710 | |||||||
chr1:44348748 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp2 HG00642.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+4102C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348748 | |||||||
chr1:44348838 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0310 |
2 | NA18952.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.211+4012C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348838 | |||||||
chr1:44348929 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.211+3921C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348929 | |||||||
chr1:44348939 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.211+3911G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348939 | |||||||
chr1:44348953 | A | G | 26 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0128 others(23): Show |
26 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+3897T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44348953 | |||||||
chr1:44349000 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.211+3850G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349000 | |||||||
chr1:44349151 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211+3699C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349151 | |||||||
chr1:44349314 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3536C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349314 | |||||||
chr1:44349488 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0090 |
4 | NA18954.hp2 NA19009.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3362A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349488 | |||||||
chr1:44349552 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+3298G>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349552 | |||||||
chr1:44349569 | C | T | 29 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0135 others(26): Show |
29 | HG01884.hp1 HG01943.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.211+3281G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349569 | |||||||
chr1:44349925 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2925G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349925 | |||||||
chr1:44349938 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+2912G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44349938 | |||||||
chr1:44350265 | CT | C | 46 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0127 others(43): Show |
46 | HG00438.hp2 HG01884.hp1 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.211+2584delA | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350265 | |||||||
chr1:44350331 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0220 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.211+2519C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350331 | |||||||
chr1:44350730 | T | G | 1 | a0001c0001t0001g0222 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+2120A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350730 | |||||||
chr1:44350743 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.211+2107C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44350743 | |||||||
chr1:44351047 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.211+1803A>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351047 | |||||||
chr1:44351432 | A | G | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(18): Show |
21 | HG00280.hp2 HG01261.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.211+1418T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351432 | |||||||
chr1:44351614 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211+1236G>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351614 | |||||||
chr1:44351626 | G | T | 70 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(67): Show |
70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.211+1224C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351626 | |||||||
chr1:44351891 | T | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+959A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44351891 | |||||||
chr1:44352093 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211+757C>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352093 | |||||||
chr1:44352159 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.211+691G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352159 | |||||||
chr1:44352369 | G | A | 4 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0335 others(1): Show |
4 | HG01261.hp2 HG03209.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+481C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352369 | |||||||
chr1:44352405 | CATAG | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(52): Show |
56 | HG00408.hp1 HG00642.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.211+441_211+444del others(4): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | |||||||
chr1:44352405 | CATAGATA others(1): Show |
C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(107): Show |
112 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.211+437_211+444del others(8): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | |||||||
chr1:44352405 | CATAGATA others(5): Show |
C | 139 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0063 others(136): Show |
139 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.211+433_211+444del others(12): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | |||||||
chr1:44352405 | CATAGATA others(9): Show |
C | 16 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0123 others(13): Show |
16 | HG00642.hp2 HG01074.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+429_211+444del others(16): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | |||||||
chr1:44352405 | CATAGATA others(13): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.211+425_211+444del others(20): Show |
ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352405 | |||||||
chr1:44352453 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211+397C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352453 | |||||||
chr1:44352462 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211+388T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352462 | |||||||
chr1:44352529 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.211+321A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352529 | |||||||
chr1:44352665 | G | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
198 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.211+185C>A | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 2/8 | chr1 | 44352665 | |||||||
chr1:44353509 | T | A | 1 | a0001c0001t0001g0003 | 2 | NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.136-584A>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44353509 | |||||||
chr1:44353703 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
233 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.136-778T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44353703 | |||||||
chr1:44353885 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.136-960T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44353885 | |||||||
chr1:44354004 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01243.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+888A>G | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354004 | |||||||
chr1:44354226 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.135+666T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354226 | |||||||
chr1:44354385 | A | G | 1 | a0001c0001t0001g0329 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+507T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354385 | |||||||
chr1:44354576 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(100): Show |
105 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.135+316C>T | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354576 | |||||||
chr1:44354647 | A | G | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.135+245T>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354647 | |||||||
chr1:44354676 | C | G | 1 | a0001c0001t0001g0004 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.135+216G>C | ERI3 | ENSG00000117419.16 | transcript | ENST00000372257.7 | protein_coding | 1/8 | chr1 | 44354676 |