geneid | 390937 |
---|---|
ensemblid | ENSG00000268041.3 |
hgncid | 53894 |
symbol | ERFL |
name | ETS repressor factor like |
refseq_nuc | NM_001365103.2 |
refseq_prot | NP_001352032.1 |
ensembl_nuc | ENST00000597630.3 |
ensembl_prot | ENSP00000491574.1 |
mane_status | MANE Select |
chr | chr19 |
start | 41907704 |
end | 41928449 |
strand | - |
ver | v1.2 |
region | chr19:41907704-41928449 |
region5000 | chr19:41902704-41933449 |
regionname0 | ERFL_chr19_41907704_41928449 |
regionname5000 | ERFL_chr19_41902704_41933449 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 11 | 0 | 2 | 5 | 0 | 4 | 2 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001 | 1/1 | 354 | 314 | 88 | 54 | 122 | 15 | 33 | 85 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0002 | 0/0 | 354 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0003 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0004 | 0/0 | 354 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0005 | 0/0 | 354 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0006 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1065 | 197 | 17 | 48 | 90 | 15 | 25 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0002 | 0/0 | 1065 | 106 | 61 | 5 | 32 | 0 | 8 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0003 | 0/0 | 1066 | 9 | 0 | 2 | 4 | 0 | 3 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0004 | 0/0 | 1065 | 9 | 9 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0005 | 0/0 | 1066 | 2 | 0 | 0 | 1 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0006 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0007 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0008 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0009 | 0/0 | 1065 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0010 | 0/0 | 1065 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0011 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
c0012 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 948 | 122 | 5 | 26 | 59 | 10 | 21 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0002 | 0/0 | 951 | 97 | 65 | 5 | 19 | 0 | 8 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0003 | 0/1 | 948 | 81 | 10 | 24 | 33 | 5 | 8 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0004 | 0/0 | 952 | 13 | 0 | 0 | 13 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0005 | 0/0 | 951 | 7 | 7 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0006 | 0/0 | 947 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0007 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0008 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0009 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0010 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0011 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0012 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0013 | 0/0 | 948 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0014 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
t0015 | 0/0 | 948 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0002 | 0/0 | 5 | 1 | 1 | 0 | 3 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0003 | 0/0 | 1066 | 9 | 0 | 2 | 4 | 0 | 3 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0000c0005 | 0/0 | 1066 | 2 | 0 | 0 | 1 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001 | 1/1 | 1065 | 197 | 17 | 48 | 90 | 15 | 25 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0002 | 0/0 | 1065 | 106 | 61 | 5 | 32 | 0 | 8 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0004 | 0/0 | 1065 | 9 | 9 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0008 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0011 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0002c0010 | 0/0 | 1065 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0003c0006 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0004c0007 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0005c0009 | 0/0 | 1065 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0006c0012 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0003t0001 | 0/0 | 2013 | 5 | 0 | 0 | 2 | 0 | 3 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0000c0003t0003 | 0/0 | 2013 | 3 | 0 | 1 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0000c0003t0015 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0000c0005t0002 | 0/0 | 2016 | 2 | 0 | 0 | 1 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0001 | 1/0 | 2012 | 114 | 5 | 25 | 56 | 10 | 17 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0003 | 0/1 | 2012 | 77 | 10 | 23 | 31 | 4 | 8 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0006 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0008 | 0/0 | 2012 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0011 | 0/0 | 2012 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0012 | 0/0 | 2012 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0013 | 0/0 | 2012 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0001t0014 | 0/0 | 2012 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0002t0002 | 0/0 | 2015 | 91 | 61 | 5 | 18 | 0 | 7 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0002t0004 | 0/0 | 2016 | 13 | 0 | 0 | 13 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0002t0009 | 0/0 | 2015 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0002t0010 | 0/0 | 2015 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0004t0002 | 0/0 | 2015 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0004t0005 | 0/0 | 2015 | 7 | 7 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0008t0001 | 0/0 | 2012 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0001c0011t0007 | 0/0 | 2015 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0002c0010t0001 | 0/0 | 2012 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0003c0006t0002 | 0/0 | 2015 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0004c0007t0001 | 0/0 | 2012 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0005c0009t0003 | 0/0 | 2012 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
a0006c0012t0002 | 0/0 | 2015 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | copy fasta | chr19 | 41902704 | 41933449 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0003t0015g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0000c0005t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0002 | 0/0 | 5 | 1 | 1 | 0 | 3 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0013g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0001t0014g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0002t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0004t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0008t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0001c0011t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0002c0010t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0003c0006t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0004c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0005c0009t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
a0006c0012t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0237 | EUR | GBR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00423 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00438 | hp1 | a0000 | c0003 | t0001 | g0170 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00544 | hp1 | a0000 | c0003 | t0003 | g0248 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00558 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00597 | hp1 | a0000 | c0003 | t0001 | g0167 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01168 | hp2 | a0000 | c0003 | t0003 | g0238 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01361 | hp2 | a0001 | c0008 | t0001 | g0057 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01891 | hp2 | a0001 | c0004 | t0005 | g0027 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01978 | hp1 | a0000 | c0003 | t0015 | g0283 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02040 | hp1 | a0001 | c0001 | t0008 | g0166 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02040 | hp2 | a0001 | c0002 | t0004 | g0019 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0205 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02132 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | CDX | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | CDX | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0198 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | KHV | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02615 | hp1 | a0001 | c0004 | t0002 | g0036 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02630 | hp2 | a0003 | c0006 | t0002 | g0124 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0146 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0193 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0027 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02970 | hp1 | a0006 | c0012 | t0002 | g0126 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0141 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02976 | hp1 | a0001 | c0011 | t0007 | g0093 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0117 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0132 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03195 | hp1 | a0001 | c0004 | t0005 | g0212 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03195 | hp2 | a0001 | c0004 | t0005 | g0213 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | ESN | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03834 | hp1 | a0001 | c0002 | t0009 | g0159 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03927 | hp1 | a0002 | c0010 | t0001 | g0056 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03927 | hp2 | a0000 | c0003 | t0001 | g0088 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04115 | hp1 | a0000 | c0003 | t0001 | g0110 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04115 | hp2 | a0000 | c0003 | t0001 | g0033 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | BEB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG04228 | hp2 | a0000 | c0005 | t0002 | g0119 | SAS | STU | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0197 | AFR | YRI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | YRI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | CHB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0080 | EAS | CHB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | CHB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CHB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | YRI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | YRI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18940 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0209 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18967 | hp2 | a0001 | c0002 | t0004 | g0161 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18982 | hp2 | a0001 | c0001 | t0014 | g0282 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0208 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18997 | hp1 | a0004 | c0007 | t0001 | g0045 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18997 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18998 | hp1 | a0001 | c0002 | t0004 | g0157 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19009 | hp1 | a0001 | c0002 | t0010 | g0145 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19030 | hp1 | a0001 | c0004 | t0005 | g0211 | AFR | LWK | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | LWK | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19079 | hp1 | a0001 | c0002 | t0004 | g0120 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19084 | hp1 | a0000 | c0005 | t0002 | g0099 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19088 | hp2 | a0001 | c0002 | t0004 | g0158 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19090 | hp1 | a0000 | c0003 | t0003 | g0279 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19091 | hp2 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | YRI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | YRI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | ASW | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20129 | hp2 | a0001 | c0004 | t0005 | g0026 | AFR | ASW | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20805 | hp1 | a0005 | c0009 | t0003 | g0242 | EUR | TSI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20805 | hp2 | a0001 | c0001 | t0013 | g0216 | EUR | TSI | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0018 | SAS | GIH | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02109 | hp1 | a0001 | c0004 | t0002 | g0035 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02109 | hp2 | a0001 | c0004 | t0005 | g0026 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0194 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ACB | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | MSL | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | USA | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | USA | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0215 | AFR | LWK | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0240 | REF | REF | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0037 | REF | REF | ERFL_chr19_41902704_41933449 | ERFL | chr19 | 41902704 | 41933449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41908239
|
T | TC | 1 | a0000 | 11 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(8): Show |
frameshift_variant | HIGH | c.1053dupG | p.Thr352fs | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1476/2012 | 1053/1065 | 351/354 | chr19 | 41908239 | ||
chr19:41908409
|
G | A | 1 | a0005 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.884C>T | p.Ala295Val | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1307/2012 | 884/1065 | 295/354 | chr19 | 41908409 | ||
chr19:41908427
|
C | T | 1 | a0004 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.866G>A | p.Arg289His | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1289/2012 | 866/1065 | 289/354 | chr19 | 41908427 | ||
chr19:41908428
|
G | A | 1 | a0003 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.865C>T | p.Arg289Cys | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1288/2012 | 865/1065 | 289/354 | chr19 | 41908428 | ||
chr19:41908586
|
G | A | 1 | a0002 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.707C>T | p.Thr236Met | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1130/2012 | 707/1065 | 236/354 | chr19 | 41908586 | ||
chr19:41909069
|
G | C | 1 | a0006 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.607C>G | p.Leu203Val | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 5/6 | 1030/2012 | 607/1065 | 203/354 | chr19 | 41909069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41908237
|
G | A | 1 | a0001c0008 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.1056C>T | p.Thr352Thr | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1479/2012 | 1056/1065 | 352/354 | chr19 | 41908237 | ||
chr19:41908387
|
T | C | 6 | a0000c0005a0001c0002a0001c0004others(3): Show | 120 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(117): Show |
synonymous_variant | LOW | c.906A>G | p.Pro302Pro | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1329/2012 | 906/1065 | 302/354 | chr19 | 41908387 | ||
chr19:41908432
|
G | A | 4 | a0000c0005a0001c0002a0003c0006others(1): Show | 110 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
synonymous_variant | LOW | c.861C>T | p.Pro287Pro | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1284/2012 | 861/1065 | 287/354 | chr19 | 41908432 | ||
chr19:41908498
|
C | T | 4 | a0000c0005a0001c0002a0003c0006others(1): Show | 110 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
synonymous_variant | LOW | c.795G>A | p.Ser265Ser | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1218/2012 | 795/1065 | 265/354 | chr19 | 41908498 | ||
chr19:41908609
|
G | C | 1 | a0001c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.684C>G | p.Pro228Pro | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 1107/2012 | 684/1065 | 228/354 | chr19 | 41908609 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41907853
|
TG | T | 10 | a0000c0005t0002a0001c0001t0006a0001c0002t0002others(7): Show | 108 | HG00438.hp2 HG00544.hp2 HG00738.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*374delC | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 374 | chr19 | 41907853 | |||||
chr19:41907905
|
C | CACAA | 10 | a0000c0005t0002a0001c0002t0002a0001c0002t0004others(7): Show | 120 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*322dupTTGT | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 322 | chr19 | 41907905 | |||||
chr19:41907987
|
G | A | 1 | a0001c0011t0007 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 241 | chr19 | 41907987 | |||||
chr19:41908077
|
C | A | 2 | a0001c0001t0008a0001c0002t0009 | 2 | HG02040.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*151G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 151 | chr19 | 41908077 | |||||
chr19:41908091
|
G | A | 1 | a0001c0002t0010 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 6/6 | 137 | chr19 | 41908091 | |||||
chr19:41928052
|
T | G | 1 | a0001c0004t0005 | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-26A>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | 15133 | chr19 | 41928052 | |||||
chr19:41928153
|
T | G | 1 | a0001c0001t0014 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127A>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | 15234 | chr19 | 41928153 | |||||
chr19:41928354
|
G | C | 1 | a0001c0001t0012 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-328C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | 15435 | chr19 | 41928354 | |||||
chr19:41928357
|
G | A | 2 | a0001c0001t0011a0001c0001t0012 | 2 | HG02559.hp1 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-331C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | 15438 | chr19 | 41928357 | |||||
chr19:41928391
|
G | C | 1 | a0001c0001t0013 | 1 | NA20805.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-365C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | chr19 | 41928391 | ||||||
chr19:41928397
|
G | C | 5 | a0000c0003t0003a0000c0003t0015a0001c0001t0003others(2): Show | 83 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-371C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | 15478 | chr19 | 41928397 | |||||
chr19:41928401
|
G | A | 1 | a0000c0003t0015 | 1 | HG01978.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-375C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/6 | chr19 | 41928401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41908772
|
G | A | 7 | a0001c0004t0002g0035a0001c0004t0002g0036a0001c0004t0005g0026others(4): Show | 9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.617-96C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 5/5 | chr19 | 41908772 | ||||||
chr19:41908905
|
A | G | 1 | a0001c0001t0003g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.616+155T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 5/5 | chr19 | 41908905 | ||||||
chr19:41908997
|
T | G | 87 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0002t0002g0001others(84): Show | 110 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.616+63A>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 5/5 | chr19 | 41908997 | ||||||
chr19:41909492
|
T | G | 1 | a0000c0003t0003g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.303-21A>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 3/5 | chr19 | 41909492 | ||||||
chr19:41909514
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.303-43G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 3/5 | chr19 | 41909514 | ||||||
chr19:41909562
|
G | A | 1 | a0001c0001t0003g0275 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.303-91C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 3/5 | chr19 | 41909562 | ||||||
chr19:41910270
|
A | G | 87 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0002t0002g0001others(84): Show | 110 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.68-173T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41910270 | ||||||
chr19:41910507
|
G | C | 1 | a0001c0002t0002g0206 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.68-410C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41910507 | ||||||
chr19:41910516
|
T | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0163others(4): Show | 7 | HG00280.hp2 HG00609.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-419A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41910516 | ||||||
chr19:41910523
|
G | A | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-426C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41910523 | ||||||
chr19:41910748
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.68-651G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41910748 | ||||||
chr19:41910837
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.68-740C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41910837 | ||||||
chr19:41911088
|
T | A | 1 | a0001c0002t0002g0039 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-991A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911088 | ||||||
chr19:41911097
|
A | C | 1 | a0001c0002t0002g0039 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-1000T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911097 | ||||||
chr19:41911202
|
A | G | 92 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0002t0002g0001others(89): Show | 117 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.68-1105T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911202 | ||||||
chr19:41911208
|
C | T | 1 | a0001c0001t0003g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.68-1111G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911208 | ||||||
chr19:41911290
|
T | C | 3 | a0001c0002t0004g0019a0001c0002t0004g0118a0001c0002t0004g0157 | 4 | HG02040.hp2 NA18940.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1193A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911290 | ||||||
chr19:41911305
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG00408.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.68-1208G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911305 | ||||||
chr19:41911513
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67+1340G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911513 | ||||||
chr19:41911578
|
CG | C | 7 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(4): Show | 9 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+1274delC | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911578 | ||||||
chr19:41911656
|
G | C | 2 | a0001c0002t0002g0090a0001c0002t0002g0092 | 2 | HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.67+1197C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911656 | ||||||
chr19:41911692
|
A | G | 1 | a0001c0002t0010g0145 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67+1161T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911692 | ||||||
chr19:41911878
|
CAT | C | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+973_67+974delAT | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911878 | ||||||
chr19:41911976
|
C | A | 1 | a0001c0001t0011g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+877G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41911976 | ||||||
chr19:41912010
|
C | T | 8 | a0001c0004t0002g0035a0001c0004t0002g0036a0001c0004t0005g0026others(5): Show | 10 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+843G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912010 | ||||||
chr19:41912015
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0003g0225a0001c0001t0003g0233others(1): Show | 4 | HG02683.hp1 HG03669.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+838G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912015 | ||||||
chr19:41912024
|
A | C | 8 | a0001c0004t0002g0035a0001c0004t0002g0036a0001c0004t0005g0026others(5): Show | 10 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+829T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912024 | ||||||
chr19:41912087
|
G | C | 3 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092 | 3 | HG02818.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.67+766C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912087 | ||||||
chr19:41912089
|
A | C | 97 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0011g0214others(94): Show | 122 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.67+764T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912089 | ||||||
chr19:41912090
|
G | A | 2 | a0001c0004t0002g0035a0001c0004t0002g0036 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+763C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912090 | ||||||
chr19:41912120
|
G | A | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+733C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912120 | ||||||
chr19:41912135
|
A | C | 1 | a0001c0002t0004g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.67+718T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912135 | ||||||
chr19:41912319
|
C | T | 1 | a0001c0001t0012g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+534G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912319 | ||||||
chr19:41912421
|
C | T | 1 | a0001c0001t0011g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+432G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912421 | ||||||
chr19:41912426
|
C | T | 1 | a0001c0002t0002g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.67+427G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912426 | ||||||
chr19:41912459
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.67+394C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912459 | ||||||
chr19:41912478
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+375G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912478 | ||||||
chr19:41912523
|
T | C | 3 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092 | 3 | HG02818.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.67+330A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912523 | ||||||
chr19:41912583
|
G | A | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67+270C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912583 | ||||||
chr19:41912585
|
G | A | 30 | a0001c0002t0002g0003a0001c0002t0002g0015a0001c0002t0002g0016others(27): Show | 36 | HG00738.hp2 HG01243.hp1 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.67+268C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912585 | ||||||
chr19:41912592
|
C | T | 1 | a0000c0003t0001g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.67+261G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912592 | ||||||
chr19:41912615
|
C | T | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+238G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912615 | ||||||
chr19:41912663
|
G | A | 1 | a0000c0003t0001g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.67+190C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 2/5 | chr19 | 41912663 | ||||||
chr19:41913060
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13-128G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913060 | ||||||
chr19:41913112
|
T | C | 140 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0001g0170others(137): Show | 171 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-13-180A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913112 | ||||||
chr19:41913281
|
C | T | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13-349G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913281 | ||||||
chr19:41913292
|
C | T | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13-360G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913292 | ||||||
chr19:41913570
|
G | C | 2 | a0001c0002t0002g0193a0001c0002t0002g0194 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-13-638C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913570 | ||||||
chr19:41913635
|
G | C | 2 | a0001c0004t0002g0035a0001c0004t0002g0036 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-703C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913635 | ||||||
chr19:41913820
|
A | G | 2 | a0001c0004t0002g0035a0001c0004t0002g0036 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-888T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913820 | ||||||
chr19:41913844
|
G | A | 1 | a0001c0001t0003g0245 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-13-912C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913844 | ||||||
chr19:41913922
|
A | C | 1 | a0001c0001t0003g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-13-990T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41913922 | ||||||
chr19:41914074
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-13-1142G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914074 | ||||||
chr19:41914079
|
A | AC | 280 | a0000c0003t0001g0033a0000c0003t0001g0088a0000c0003t0001g0110others(277): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-13-1148dupG | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914079 | ||||||
chr19:41914220
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-13-1288G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914220 | ||||||
chr19:41914237
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-13-1305C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914237 | ||||||
chr19:41914403
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-13-1471C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914403 | ||||||
chr19:41914453
|
T | C | 101 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0072others(98): Show | 128 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-13-1521A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914453 | ||||||
chr19:41914497
|
G | A | 1 | a0001c0002t0002g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-13-1565C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914497 | ||||||
chr19:41914538
|
ATCCGTCT others(26): Show |
A | 2 | a0001c0001t0001g0207a0001c0001t0003g0235 | 2 | HG02630.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-13-1639_-13-1607d others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914538 | ||||||
chr19:41914541
|
CGTCTTTC others(113): Show |
C | 1 | a0001c0001t0012g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13-1729_-13-1610d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914541 | ||||||
chr19:41914541
|
CGTCTTTC others(140): Show |
C | 3 | a0001c0002t0002g0112a0001c0002t0002g0114a0001c0002t0002g0134 | 3 | HG02647.hp1 HG02809.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-13-1756_-13-1610d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914541 | ||||||
chr19:41914541
|
CGTCTTTC others(194): Show |
C | 1 | a0001c0002t0002g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-13-1810_-13-1610d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914541 | ||||||
chr19:41914546
|
T | A | 1 | a0001c0001t0003g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-13-1614A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
T | C | 8 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0155others(5): Show | 8 | HG00280.hp1 HG01361.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-1614A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
T | TTCCCTCC others(20): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0179 | 2 | NA18964.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-13-1641_-13-1615d others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
T | TTCCCTCC others(93): Show |
1 | a0001c0001t0001g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-13-1615_-13-1614i others(102): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
T | TTCCCTCC others(47): Show |
1 | a0001c0002t0004g0208 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-13-1615_-13-1614i others(56): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
T | TTCCCTCC others(228): Show |
1 | a0001c0001t0001g0062 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-13-1615_-13-1614i others(237): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
T | TTCCCTCC others(242): Show |
1 | a0001c0001t0001g0192 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-13-1615_-13-1614i others(251): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
TTCCCTCC others(113): Show |
T | 5 | a0001c0001t0001g0041a0001c0001t0001g0073a0001c0002t0002g0131others(2): Show | 5 | HG00323.hp1 HG02818.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1734_-13-1615d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
TTCCCTCC others(140): Show |
T | 1 | a0001c0001t0003g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-13-1761_-13-1615d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
TTCCCTCC others(167): Show |
T | 5 | a0001c0002t0002g0039a0001c0002t0002g0100a0001c0002t0002g0193others(2): Show | 5 | HG01109.hp2 HG02922.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-1788_-13-1615d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914546
|
TTCCCTCC others(194): Show |
T | 1 | a0001c0001t0001g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-13-1815_-13-1615d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914546 | ||||||
chr19:41914555
|
C | CTTCCACC others(194): Show |
1 | a0001c0001t0003g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-13-1624_-13-1623i others(203): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914555 | ||||||
chr19:41914555
|
C | T | 22 | a0001c0001t0001g0151a0001c0001t0001g0155a0001c0001t0001g0175others(19): Show | 27 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.-13-1623G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914555 | ||||||
chr19:41914555
|
CTTCCACC others(26): Show |
C | 17 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0082others(14): Show | 20 | HG00423.hp2 HG00621.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13-1656_-13-1624d others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914555 | ||||||
chr19:41914555
|
CTTCCACC others(86): Show |
C | 7 | a0001c0001t0001g0074a0001c0001t0003g0236a0001c0001t0003g0261others(4): Show | 7 | HG01099.hp1 HG01258.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-1716_-13-1624d others(95): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914555 | ||||||
chr19:41914556
|
T | TTCCACCA others(93): Show |
1 | a0001c0004t0002g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-13-1625_-13-1624i others(102): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914556 | ||||||
chr19:41914556
|
TTCCACCA others(294): Show |
T | 4 | a0001c0001t0001g0024a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG00408.hp1 HG02027.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1925_-13-1625d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914556 | ||||||
chr19:41914562
|
CATCTCT | C | 8 | a0001c0001t0003g0009a0001c0001t0003g0230a0001c0001t0003g0265others(5): Show | 10 | HG02145.hp2 HG02572.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-1636_-13-1631d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914562 | ||||||
chr19:41914562
|
CATCTCTG others(59): Show |
C | 1 | a0001c0002t0002g0149 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-13-1696_-13-1631d others(68): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914562 | ||||||
chr19:41914563
|
A | G | 1 | a0001c0001t0003g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-13-1631T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914563 | ||||||
chr19:41914563
|
ATCTCTGT others(59): Show |
A | 10 | a0000c0003t0001g0088a0001c0001t0001g0050a0001c0001t0001g0075others(7): Show | 10 | HG00733.hp1 HG02132.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-1697_-13-1632d others(68): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914563 | ||||||
chr19:41914563
|
ATCTCTGT others(194): Show |
A | 8 | a0000c0003t0015g0283a0001c0001t0001g0014a0001c0001t0003g0006others(5): Show | 12 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-1832_-13-1632d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914563 | ||||||
chr19:41914568
|
T | TGTCTCTC others(19): Show |
1 | a0001c0001t0001g0044 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-13-1637_-13-1636i others(28): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914568 | ||||||
chr19:41914568
|
T | TGTCTCTC others(161): Show |
1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13-1637_-13-1636i others(170): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914568 | ||||||
chr19:41914568
|
T | TGTCTCTC others(107): Show |
1 | a0001c0001t0003g0257 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-13-1637_-13-1636i others(116): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914568 | ||||||
chr19:41914568
|
TGTCTCC | T | 105 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0003g0238others(102): Show | 127 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-13-1642_-13-1637d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914568 | ||||||
chr19:41914568
|
TGTCTCCG others(188): Show |
T | 1 | a0001c0002t0002g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-13-1831_-13-1637d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914568 | ||||||
chr19:41914569
|
G | GTCTCTCC others(95): Show |
1 | a0001c0001t0001g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(104): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(14): Show |
1 | a0001c0001t0001g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(41): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0094a0001c0001t0001g0097 | 3 | HG01070.hp1 HG01243.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-13-1638_-13-1637i others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(68): Show |
1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(77): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(122): Show |
1 | a0001c0001t0001g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(131): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(182): Show |
1 | a0001c0001t0003g0276 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(191): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(94): Show |
1 | a0001c0001t0001g0183 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(103): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(122): Show |
1 | a0001c0001t0003g0267 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(131): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(155): Show |
1 | a0001c0001t0001g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(164): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(68): Show |
2 | a0001c0001t0001g0052a0001c0001t0013g0216 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-13-1638_-13-1637i others(77): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(80): Show |
1 | a0001c0001t0001g0053 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(89): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
G | GTCTCTCC others(14): Show |
1 | a0001c0001t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-13-1638_-13-1637i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
GTCTCCGT others(80): Show |
G | 2 | a0001c0002t0002g0147a0001c0002t0002g0199 | 2 | HG01981.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-13-1724_-13-1638d others(89): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914569
|
GTCTCCGT others(106): Show |
G | 2 | a0001c0002t0002g0025a0001c0002t0002g0031 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-13-1750_-13-1638d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914569 | ||||||
chr19:41914572
|
T | TCTCCCTC others(8): Show |
1 | a0001c0001t0001g0187 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-13-1641_-13-1640i others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914572 | ||||||
chr19:41914572
|
T | TCTCCCTC others(35): Show |
1 | a0001c0001t0003g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-13-1641_-13-1640i others(44): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914572 | ||||||
chr19:41914572
|
T | TCTCCCTC others(35): Show |
1 | a0000c0003t0001g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-13-1641_-13-1640i others(44): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914572 | ||||||
chr19:41914574
|
C | T | 59 | a0000c0003t0003g0248a0000c0003t0003g0279a0001c0001t0001g0044others(56): Show | 61 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-13-1642G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914574 | ||||||
chr19:41914574
|
CGTCTCTC others(53): Show |
C | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-13-1702_-13-1643d others(62): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914574 | ||||||
chr19:41914574
|
CGTCTCTC others(80): Show |
C | 1 | a0001c0002t0002g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-13-1729_-13-1643d others(89): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914574 | ||||||
chr19:41914574
|
CGTCTCTC others(107): Show |
C | 7 | a0001c0002t0002g0007a0001c0002t0002g0111a0001c0002t0002g0130others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13-1756_-13-1643d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914574 | ||||||
chr19:41914577
|
C | G | 3 | a0000c0003t0001g0033a0001c0001t0001g0187a0001c0001t0003g0229 | 3 | HG03130.hp2 HG04115.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-13-1645G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914577 | ||||||
chr19:41914579
|
C | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0192a0001c0002t0002g0121 | 3 | HG02055.hp2 NA19058.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-13-1647G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914579 | ||||||
chr19:41914579
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0003g0256a0001c0002t0002g0196others(1): Show | 4 | HG01884.hp1 HG01884.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1647G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914579 | ||||||
chr19:41914582
|
C | G | 1 | a0001c0004t0002g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-13-1650G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914582 | ||||||
chr19:41914584
|
T | C | 4 | a0000c0003t0001g0033a0001c0001t0001g0187a0001c0001t0003g0229others(1): Show | 4 | HG02698.hp2 HG03130.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-1652A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914584 | ||||||
chr19:41914584
|
TCCCTTTC others(236): Show |
T | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-13-1895_-13-1653d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914584 | ||||||
chr19:41914587
|
CT | C | 3 | a0001c0001t0003g0218a0001c0001t0003g0220a0001c0002t0002g0092 | 3 | HG00621.hp2 HG02135.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-13-1656delA | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914587 | ||||||
chr19:41914588
|
T | C | 151 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0003g0238others(148): Show | 176 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.-13-1656A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914588 | ||||||
chr19:41914588
|
T | TTTCCACC others(47): Show |
1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-13-1657_-13-1656i others(56): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914588 | ||||||
chr19:41914589
|
T | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0044others(13): Show | 20 | HG00280.hp1 HG00621.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-13-1657A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914589 | ||||||
chr19:41914589
|
TTCCACCA others(261): Show |
T | 7 | a0000c0003t0001g0170a0001c0001t0001g0005a0001c0001t0001g0104others(4): Show | 14 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13-1925_-13-1658d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914589 | ||||||
chr19:41914594
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0220 | 2 | HG00621.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-13-1662G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914594 | ||||||
chr19:41914595
|
CATCTCT | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(2): Show | 7 | HG01258.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1669_-13-1664d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914595 | ||||||
chr19:41914595
|
CATCTCTG others(293): Show |
C | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-13-1963_-13-1664d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914595 | ||||||
chr19:41914596
|
A | ATCTCTG | 7 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0232others(4): Show | 7 | HG00642.hp1 HG01358.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-1670_-13-1665d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914596 | ||||||
chr19:41914596
|
A | G | 21 | a0000c0003t0001g0033a0001c0001t0001g0008a0001c0001t0001g0052others(18): Show | 24 | HG00558.hp2 HG00642.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13-1664T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914596 | ||||||
chr19:41914601
|
TGTCTCTC others(230): Show |
T | 1 | a0001c0002t0002g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-13-1906_-13-1670d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914601 | ||||||
chr19:41914602
|
GTCTCTCC others(47): Show |
G | 1 | a0001c0001t0001g0013 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-13-1724_-13-1671d others(56): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914602 | ||||||
chr19:41914602
|
GTCTCTCC others(74): Show |
G | 3 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0213 | 5 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-1751_-13-1671d others(83): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914602 | ||||||
chr19:41914602
|
GTCTCTCC others(101): Show |
G | 4 | a0001c0001t0001g0070a0001c0001t0003g0256a0001c0004t0005g0211others(1): Show | 4 | HG01884.hp1 HG02165.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1778_-13-1671d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914602 | ||||||
chr19:41914602
|
GTCTCTCC others(128): Show |
G | 1 | a0001c0001t0001g0067 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-13-1805_-13-1671d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914602 | ||||||
chr19:41914604
|
C | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(2): Show | 7 | HG01258.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1672G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914604 | ||||||
chr19:41914606
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0186 | 2 | NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-1674G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914606 | ||||||
chr19:41914609
|
CCT | C | 5 | a0000c0003t0001g0033a0001c0001t0001g0187a0001c0001t0003g0218others(2): Show | 6 | HG00621.hp2 HG03130.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1679_-13-1678d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914609 | ||||||
chr19:41914611
|
T | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(2): Show | 7 | HG01258.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1679A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914611 | ||||||
chr19:41914611
|
T | TCCCCCTC others(12): Show |
1 | a0001c0001t0001g0048 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-13-1680_-13-1679i others(21): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914611 | ||||||
chr19:41914611
|
T | TCCCCCTC others(39): Show |
2 | a0001c0002t0002g0150a0001c0002t0002g0190 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13-1680_-13-1679i others(48): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914611 | ||||||
chr19:41914614
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-13-1682G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914614 | ||||||
chr19:41914615
|
C | CCTCCACC others(14): Show |
1 | a0001c0001t0003g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-13-1684_-13-1683i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914615 | ||||||
chr19:41914615
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(11): Show | 16 | HG00642.hp1 HG01258.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-1683G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914615 | ||||||
chr19:41914616
|
T | C | 67 | a0000c0003t0001g0033a0000c0003t0001g0167a0000c0005t0002g0099others(64): Show | 92 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-13-1684A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914616 | ||||||
chr19:41914616
|
TTCCACCA others(234): Show |
T | 1 | a0001c0001t0001g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-13-1925_-13-1685d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914616 | ||||||
chr19:41914621
|
C | T | 2 | a0001c0001t0001g0192a0001c0004t0002g0035 | 2 | HG02109.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-13-1689G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914621 | ||||||
chr19:41914622
|
CATCTCT | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0046others(8): Show | 13 | HG00558.hp2 HG01258.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1696_-13-1691d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914622 | ||||||
chr19:41914622
|
CATCTCTG others(5): Show |
C | 51 | a0000c0003t0001g0167a0000c0005t0002g0099a0000c0005t0002g0119others(48): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-13-1702_-13-1691d others(14): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914622 | ||||||
chr19:41914622
|
CATCTCTG others(266): Show |
C | 2 | a0001c0001t0003g0227a0001c0001t0003g0264 | 2 | HG01069.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-13-1963_-13-1691d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914622 | ||||||
chr19:41914623
|
A | G | 6 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0003g0239others(3): Show | 6 | HG01346.hp1 HG01358.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-1691T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914623 | ||||||
chr19:41914623
|
ATCTCTG | A | 33 | a0000c0003t0003g0238a0001c0001t0001g0043a0001c0001t0001g0044others(30): Show | 33 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-13-1697_-13-1692d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914623 | ||||||
chr19:41914623
|
ATCTCTGT others(161): Show |
A | 1 | a0001c0002t0002g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-13-1859_-13-1692d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914623 | ||||||
chr19:41914628
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0048others(3): Show | 8 | HG00280.hp1 HG00642.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-1696A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914628 | ||||||
chr19:41914628
|
T | TGTCTCTC others(14): Show |
1 | a0001c0001t0001g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-13-1697_-13-1696i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914628 | ||||||
chr19:41914628
|
T | TGTCTCTC others(41): Show |
1 | a0001c0001t0001g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-13-1697_-13-1696i others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914628 | ||||||
chr19:41914629
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-13-1697C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(152): Show |
1 | a0001c0004t0002g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(161): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(14): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0180 | 3 | HG02155.hp1 NA18964.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-13-1698_-13-1697i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(41): Show |
1 | a0001c0001t0001g0181 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(203): Show |
1 | a0001c0001t0001g0042 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(212): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(392): Show |
1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(401): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(68): Show |
1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(77): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(287): Show |
1 | a0001c0001t0001g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(296): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
G | GTCTCTCC others(563): Show |
1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13-1698_-13-1697i others(572): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
GTCTCTGT others(20): Show |
G | 1 | a0001c0001t0003g0266 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-13-1724_-13-1698d others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914629
|
GTCTCTGT others(101): Show |
G | 3 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0003g0246 | 3 | HG01106.hp1 HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-13-1805_-13-1698d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914629 | ||||||
chr19:41914634
|
T | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0072a0001c0001t0001g0095others(8): Show | 11 | HG00609.hp1 HG01109.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-1702A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914634 | ||||||
chr19:41914634
|
T | TCCCTCCC others(8): Show |
1 | a0001c0001t0003g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13-1703_-13-1702i others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914634 | ||||||
chr19:41914635
|
G | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1703C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914635 | ||||||
chr19:41914636
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1704A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914636 | ||||||
chr19:41914637
|
C | G | 52 | a0000c0003t0001g0167a0000c0005t0002g0099a0000c0005t0002g0119others(49): Show | 73 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-13-1705G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914637 | ||||||
chr19:41914639
|
C | A | 14 | a0000c0003t0001g0110a0000c0003t0003g0248a0000c0003t0003g0279others(11): Show | 14 | HG00544.hp1 HG01952.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13-1707G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914639 | ||||||
chr19:41914639
|
C | T | 5 | a0001c0001t0003g0218a0001c0001t0003g0220a0001c0001t0003g0229others(2): Show | 5 | HG00621.hp2 HG02135.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1707G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914639 | ||||||
chr19:41914639
|
CT | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1708delA | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914639 | ||||||
chr19:41914640
|
T | C | 2 | a0001c0002t0002g0127a0006c0012t0002g0126 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-1708A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914640 | ||||||
chr19:41914642
|
C | G | 2 | a0001c0001t0001g0187a0001c0002t0002g0190 | 2 | NA19005.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13-1710G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914642 | ||||||
chr19:41914644
|
T | C | 58 | a0000c0003t0001g0167a0000c0005t0002g0099a0000c0005t0002g0119others(55): Show | 81 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-13-1712A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914644 | ||||||
chr19:41914647
|
C | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1715G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914647 | ||||||
chr19:41914647
|
C | T | 1 | a0001c0004t0002g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-13-1715G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914647 | ||||||
chr19:41914647
|
CTT | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(2): Show | 7 | HG01258.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1717_-13-1716d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914647 | ||||||
chr19:41914648
|
T | C | 121 | a0000c0003t0001g0033a0000c0003t0001g0088a0000c0003t0001g0110others(118): Show | 125 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-13-1716A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914648 | ||||||
chr19:41914649
|
T | C | 12 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0105others(9): Show | 12 | HG00558.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13-1717A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914649 | ||||||
chr19:41914649
|
T | TTCCACCA others(41): Show |
1 | a0001c0001t0001g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-13-1718_-13-1717i others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914649 | ||||||
chr19:41914649
|
TTCCACCA others(201): Show |
T | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13-1925_-13-1718d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914649 | ||||||
chr19:41914650
|
T | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1718A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914650 | ||||||
chr19:41914651
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1719G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914651 | ||||||
chr19:41914653
|
A | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0178a0001c0001t0001g0183 | 3 | HG01496.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13-1721T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914653 | ||||||
chr19:41914654
|
C | CCGTCTCT others(46): Show |
1 | a0001c0001t0001g0068 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-13-1723_-13-1722i others(55): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914654 | ||||||
chr19:41914654
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0011g0214 | 2 | HG02559.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-13-1722G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914654 | ||||||
chr19:41914655
|
C | CGTCTCTG others(26): Show |
1 | a0001c0001t0001g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-13-1724_-13-1723i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914655 | ||||||
chr19:41914655
|
C | T | 1 | a0001c0004t0002g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-13-1723G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914655 | ||||||
chr19:41914655
|
CATCTCTG others(233): Show |
C | 6 | a0001c0001t0001g0151a0001c0001t0001g0207a0001c0001t0003g0247others(3): Show | 6 | HG01993.hp1 HG02630.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1963_-13-1724d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914655 | ||||||
chr19:41914656
|
A | ATCTCCG | 3 | a0001c0001t0001g0059a0001c0001t0003g0252a0001c0001t0003g0253 | 3 | HG00558.hp2 HG02004.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-13-1725_-13-1724i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914656 | ||||||
chr19:41914656
|
A | ATCTCCGT others(59): Show |
1 | a0001c0001t0001g0055 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-13-1725_-13-1724i others(68): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914656 | ||||||
chr19:41914656
|
A | ATCTCTG | 10 | a0000c0003t0001g0110a0001c0001t0001g0053a0001c0001t0001g0076others(7): Show | 10 | HG01346.hp2 HG01361.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-1730_-13-1725d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914656 | ||||||
chr19:41914656
|
A | ATCTCTGT others(26): Show |
1 | a0001c0001t0003g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-13-1757_-13-1725d others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914656 | ||||||
chr19:41914656
|
A | ATCTCTGT others(59): Show |
1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13-1725_-13-1724i others(68): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914656 | ||||||
chr19:41914656
|
A | G | 84 | a0000c0003t0001g0167a0000c0003t0003g0279a0000c0005t0002g0099others(81): Show | 106 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13-1724T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914656 | ||||||
chr19:41914661
|
T | TGTCTCTC others(134): Show |
1 | a0001c0001t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-13-1730_-13-1729i others(143): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914661 | ||||||
chr19:41914661
|
TGTCTCTC others(170): Show |
T | 2 | a0001c0001t0001g0008a0001c0001t0001g0105 | 4 | HG00642.hp2 NA18980.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1906_-13-1730d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914661 | ||||||
chr19:41914662
|
GTCTCTCC others(14): Show |
G | 2 | a0001c0001t0014g0282a0001c0002t0002g0143 | 2 | NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-13-1751_-13-1731d others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914662 | ||||||
chr19:41914662
|
GTCTCTCC others(41): Show |
G | 2 | a0001c0001t0001g0106a0001c0002t0002g0148 | 2 | HG03688.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-13-1778_-13-1731d others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914662 | ||||||
chr19:41914662
|
GTCTCTCC others(68): Show |
G | 4 | a0000c0003t0001g0167a0001c0001t0001g0060a0001c0001t0001g0096others(1): Show | 4 | HG00597.hp1 HG01346.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-1805_-13-1731d others(77): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914662 | ||||||
chr19:41914664
|
C | G | 1 | a0001c0002t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-13-1732G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914664 | ||||||
chr19:41914666
|
C | A | 3 | a0001c0001t0003g0252a0001c0002t0002g0133a0001c0002t0002g0147 | 3 | HG00558.hp2 HG01261.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-13-1734G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914666 | ||||||
chr19:41914666
|
C | T | 1 | a0000c0003t0001g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-13-1734G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914666 | ||||||
chr19:41914668
|
C | G | 2 | a0001c0002t0002g0127a0006c0012t0002g0126 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-1736G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914668 | ||||||
chr19:41914669
|
C | T | 3 | a0001c0001t0003g0218a0001c0002t0002g0127a0006c0012t0002g0126 | 3 | HG00621.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-1737G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914669 | ||||||
chr19:41914669
|
CCT | C | 49 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0142others(46): Show | 70 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-13-1739_-13-1738d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914669 | ||||||
chr19:41914671
|
T | C | 1 | a0001c0002t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-13-1739A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914671 | ||||||
chr19:41914671
|
TCCCCTTC others(202): Show |
T | 1 | a0001c0002t0002g0021 | 2 | NA18747.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-13-1948_-13-1740d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914671 | ||||||
chr19:41914675
|
C | CCTCCACC others(14): Show |
1 | a0001c0002t0002g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-13-1744_-13-1743i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914675 | ||||||
chr19:41914675
|
C | T | 14 | a0000c0003t0001g0110a0001c0001t0001g0078a0001c0001t0001g0169others(11): Show | 14 | HG00609.hp1 HG00609.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13-1743G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914675 | ||||||
chr19:41914676
|
T | C | 76 | a0000c0003t0003g0248a0000c0003t0003g0279a0000c0005t0002g0099others(73): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-13-1744A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914676 | ||||||
chr19:41914676
|
TTCCACCA others(174): Show |
T | 2 | a0001c0001t0003g0240a0001c0001t0003g0243 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-13-1925_-13-1745d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914676 | ||||||
chr19:41914677
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-13-1745A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914677 | ||||||
chr19:41914680
|
A | T | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-13-1748T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914680 | ||||||
chr19:41914681
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0003g0221 | 2 | NA18954.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-1749G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914681 | ||||||
chr19:41914682
|
C | CGTCTCTG others(325): Show |
1 | a0001c0001t0001g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-13-1751_-13-1750i others(334): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914682 | ||||||
chr19:41914682
|
C | CGTGTCTC others(20): Show |
1 | a0001c0001t0001g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-13-1751_-13-1750i others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914682 | ||||||
chr19:41914682
|
CATCTCT | C | 7 | a0001c0001t0001g0176a0001c0001t0003g0236a0001c0001t0003g0269others(4): Show | 7 | HG01258.hp2 HG02074.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1756_-13-1751d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914682 | ||||||
chr19:41914682
|
CATCTCTG others(206): Show |
C | 1 | a0001c0001t0003g0029 | 2 | HG01361.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-13-1963_-13-1751d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914682 | ||||||
chr19:41914683
|
A | ATCTCCG | 11 | a0000c0003t0003g0248a0000c0003t0003g0279a0001c0001t0001g0032others(8): Show | 11 | HG00544.hp1 HG01496.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-1752_-13-1751i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914683 | ||||||
chr19:41914683
|
A | ATCTCTG | 13 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0051others(10): Show | 14 | HG01070.hp1 HG01975.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13-1757_-13-1752d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914683 | ||||||
chr19:41914683
|
A | ATCTCTGT others(26): Show |
1 | a0001c0001t0003g0028 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-13-1752_-13-1751i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914683 | ||||||
chr19:41914683
|
A | C | 2 | a0001c0002t0002g0025a0001c0002t0002g0031 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-13-1751T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914683 | ||||||
chr19:41914683
|
A | G | 21 | a0000c0003t0003g0238a0001c0001t0001g0013a0001c0001t0001g0052others(18): Show | 21 | HG01168.hp2 HG01243.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13-1751T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914683 | ||||||
chr19:41914685
|
C | A | 2 | a0001c0002t0002g0025a0001c0002t0002g0031 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-13-1753G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914685 | ||||||
chr19:41914686
|
TCTGTCTC others(14): Show |
T | 1 | a0001c0002t0002g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13-1775_-13-1755d others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914686 | ||||||
chr19:41914686
|
TCTGTCTC others(41): Show |
T | 1 | a0001c0001t0003g0231 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-13-1802_-13-1755d others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914686 | ||||||
chr19:41914686
|
TCTGTCTC others(68): Show |
T | 2 | a0001c0001t0001g0101a0001c0002t0002g0156 | 2 | NA18986.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-1829_-13-1755d others(77): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914686 | ||||||
chr19:41914688
|
T | C | 2 | a0001c0002t0002g0025a0001c0002t0002g0031 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-13-1756A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914688 | ||||||
chr19:41914688
|
TGTCTCTC others(68): Show |
T | 3 | a0001c0001t0001g0012a0001c0001t0001g0084a0001c0001t0003g0252 | 4 | HG00558.hp2 NA19064.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1831_-13-1757d others(77): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914688 | ||||||
chr19:41914688
|
TGTCTCTC others(143): Show |
T | 38 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0142others(35): Show | 56 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.-13-1906_-13-1757d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914688 | ||||||
chr19:41914689
|
GTCTCTCC others(14): Show |
G | 4 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0085others(1): Show | 4 | HG02004.hp1 HG02129.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1778_-13-1758d others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914689 | ||||||
chr19:41914689
|
GTCTCTCC others(41): Show |
G | 6 | a0001c0001t0001g0013a0001c0001t0001g0082a0001c0001t0003g0250others(3): Show | 6 | HG00408.hp2 HG01261.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-1805_-13-1758d others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914689 | ||||||
chr19:41914691
|
C | G | 7 | a0001c0001t0001g0176a0001c0001t0003g0236a0001c0001t0003g0269others(4): Show | 7 | HG01258.hp2 HG02074.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1759G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914691 | ||||||
chr19:41914693
|
C | A | 4 | a0001c0001t0001g0195a0001c0004t0005g0026a0001c0004t0005g0027others(1): Show | 6 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1761G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914693 | ||||||
chr19:41914693
|
C | CCGTCTT | 5 | a0001c0001t0003g0009a0001c0001t0003g0230a0001c0001t0003g0265others(2): Show | 7 | HG02145.hp2 HG02970.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1762_-13-1761i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914693 | ||||||
chr19:41914693
|
C | T | 8 | a0001c0002t0002g0007a0001c0002t0002g0025a0001c0002t0002g0031others(5): Show | 11 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-1761G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914693 | ||||||
chr19:41914694
|
TCCCTCCC others(116): Show |
T | 1 | a0001c0001t0001g0168 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-13-1885_-13-1763d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914694 | ||||||
chr19:41914696
|
C | T | 1 | a0001c0001t0008g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-13-1764G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914696 | ||||||
chr19:41914698
|
T | C | 8 | a0001c0001t0001g0176a0001c0001t0003g0236a0001c0001t0003g0269others(5): Show | 8 | HG01258.hp2 HG02040.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-1766A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914698 | ||||||
chr19:41914699
|
CCCCTTCC others(173): Show |
C | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-13-1947_-13-1768d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914699 | ||||||
chr19:41914701
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0204 | 2 | HG01496.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-13-1769G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914701 | ||||||
chr19:41914702
|
C | CCTCCACC others(14): Show |
2 | a0001c0002t0002g0150a0001c0002t0002g0190 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13-1771_-13-1770i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914702 | ||||||
chr19:41914702
|
C | CCTCCACC others(72): Show |
1 | a0001c0001t0003g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-13-1771_-13-1770i others(81): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914702 | ||||||
chr19:41914702
|
C | T | 18 | a0001c0001t0001g0078a0001c0001t0001g0103a0001c0001t0001g0163others(15): Show | 18 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13-1770G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914702 | ||||||
chr19:41914703
|
T | C | 17 | a0000c0003t0001g0033a0000c0003t0003g0248a0000c0003t0003g0279others(14): Show | 17 | HG00280.hp1 HG00544.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13-1771A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914703 | ||||||
chr19:41914704
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-13-1772A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914704 | ||||||
chr19:41914707
|
A | ACCGTGTC others(78): Show |
1 | a0001c0001t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-1776_-13-1775i others(87): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914707 | ||||||
chr19:41914707
|
A | T | 1 | a0001c0001t0001g0184 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-13-1775T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914707 | ||||||
chr19:41914708
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0003g0223 | 2 | HG03834.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-13-1776G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914708 | ||||||
chr19:41914709
|
C | CGTCTCT | 4 | a0001c0001t0001g0069a0001c0001t0003g0241a0001c0001t0003g0269others(1): Show | 4 | HG03491.hp1 NA18980.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1778_-13-1777i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914709 | ||||||
chr19:41914709
|
CATCTCTG others(179): Show |
C | 1 | a0001c0001t0001g0187 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-13-1963_-13-1778d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914709 | ||||||
chr19:41914710
|
A | ATCTCCG | 7 | a0000c0003t0003g0248a0000c0003t0003g0279a0001c0001t0001g0179others(4): Show | 7 | HG00544.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1779_-13-1778i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914710 | ||||||
chr19:41914710
|
A | ATCTCTG | 13 | a0000c0003t0001g0110a0001c0001t0001g0071a0001c0001t0001g0182others(10): Show | 13 | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1784_-13-1779d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914710 | ||||||
chr19:41914710
|
A | ATCTCTGT others(26): Show |
1 | a0001c0001t0003g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-13-1811_-13-1779d others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914710 | ||||||
chr19:41914710
|
A | ATCTCTGT others(20): Show |
1 | a0001c0001t0001g0044 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-13-1779_-13-1778i others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914710 | ||||||
chr19:41914710
|
A | ATCTCTGT others(101): Show |
1 | a0001c0001t0003g0239 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-13-1779_-13-1778i others(110): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914710 | ||||||
chr19:41914710
|
A | G | 45 | a0000c0003t0003g0238a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 49 | HG00423.hp2 HG00621.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.-13-1778T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914710 | ||||||
chr19:41914712
|
C | GTCTGTCT others(26): Show |
1 | a0001c0001t0001g0097 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-13-1780_-13-1779i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914712 | ||||||
chr19:41914713
|
TCTGTCTC others(14): Show |
T | 1 | a0001c0001t0003g0245 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-13-1802_-13-1782d others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914713 | ||||||
chr19:41914713
|
TCTGTCTC others(141): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-13-1929_-13-1782d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914713 | ||||||
chr19:41914715
|
T | C | 1 | a0001c0001t0003g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-13-1783A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914715 | ||||||
chr19:41914715
|
TGTCTCTC others(41): Show |
T | 3 | a0001c0001t0001g0032a0001c0001t0001g0152a0001c0001t0008g0166 | 3 | HG02040.hp1 HG02074.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-13-1831_-13-1784d others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914715 | ||||||
chr19:41914715
|
TGTCTCTC others(116): Show |
T | 2 | a0001c0001t0003g0220a0001c0002t0002g0139 | 2 | HG02135.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-13-1906_-13-1784d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914715 | ||||||
chr19:41914716
|
GTCTCTCC others(14): Show |
G | 4 | a0001c0001t0001g0013a0001c0001t0003g0266a0001c0001t0003g0281others(1): Show | 4 | HG01993.hp2 NA18612.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1805_-13-1785d others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914716 | ||||||
chr19:41914718
|
C | G | 2 | a0001c0001t0003g0233a0001c0002t0002g0196 | 2 | HG01884.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-13-1786G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914718 | ||||||
chr19:41914720
|
C | A | 3 | a0001c0001t0001g0103a0001c0001t0003g0219a0001c0001t0003g0235 | 3 | HG03831.hp2 NA18964.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-13-1788G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914720 | ||||||
chr19:41914720
|
C | CTGTCTA | 4 | a0001c0001t0001g0178a0001c0001t0003g0225a0001c0001t0003g0228others(1): Show | 5 | HG01496.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-1789_-13-1788i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914720 | ||||||
chr19:41914723
|
C | G | 2 | a0001c0002t0002g0116a0001c0002t0002g0148 | 2 | HG02886.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-13-1791G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914723 | ||||||
chr19:41914723
|
CCT | C | 5 | a0001c0001t0001g0176a0001c0001t0003g0236a0001c0002t0002g0150others(2): Show | 5 | HG01258.hp2 HG02074.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1793_-13-1792d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914723 | ||||||
chr19:41914725
|
T | C | 2 | a0001c0001t0003g0233a0001c0002t0002g0196 | 2 | HG01884.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-13-1793A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914725 | ||||||
chr19:41914728
|
C | T | 5 | a0001c0001t0001g0179a0001c0001t0001g0204a0001c0002t0002g0200others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1796G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914728 | ||||||
chr19:41914729
|
C | CCTCCACC others(14): Show |
1 | a0000c0003t0003g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-13-1798_-13-1797i others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914729 | ||||||
chr19:41914729
|
C | T | 12 | a0001c0001t0001g0078a0001c0001t0001g0106a0001c0001t0001g0163others(9): Show | 12 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13-1797G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914729 | ||||||
chr19:41914730
|
T | C | 19 | a0000c0003t0003g0248a0000c0003t0003g0279a0001c0001t0001g0155others(16): Show | 21 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13-1798A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914730 | ||||||
chr19:41914730
|
TTCCACCA others(120): Show |
T | 1 | a0001c0001t0001g0078 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-13-1925_-13-1799d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914730 | ||||||
chr19:41914734
|
A | ACCGTGTC others(71): Show |
1 | a0004c0007t0001g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-13-1803_-13-1802i others(80): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914734 | ||||||
chr19:41914735
|
C | T | 2 | a0001c0001t0003g0262a0001c0002t0002g0160 | 2 | HG02523.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-13-1803G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914735 | ||||||
chr19:41914736
|
C | CGTCTCTG others(26): Show |
2 | a0000c0003t0001g0033a0001c0001t0001g0048 | 2 | HG04115.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.-13-1805_-13-1804i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914736 | ||||||
chr19:41914736
|
C | T | 4 | a0001c0001t0001g0204a0001c0002t0002g0200a0001c0004t0002g0035others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1804G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914736 | ||||||
chr19:41914736
|
CATCTCTG others(152): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-13-1963_-13-1805d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914736 | ||||||
chr19:41914737
|
A | ATCTCCG | 3 | a0000c0003t0003g0248a0001c0001t0001g0195a0001c0001t0003g0272 | 3 | HG00423.hp2 HG00544.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-13-1806_-13-1805i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTG | 29 | a0000c0003t0001g0088a0000c0003t0001g0110a0001c0001t0001g0038others(26): Show | 30 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-13-1811_-13-1806d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(26): Show |
1 | a0001c0001t0003g0276 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(72): Show |
1 | a0006c0012t0002g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(81): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(26): Show |
2 | a0001c0001t0001g0089a0001c0001t0003g0267 | 2 | HG02683.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-13-1806_-13-1805i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(269): Show |
1 | a0001c0001t0001g0079 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(278): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(86): Show |
1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(95): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(86): Show |
1 | a0001c0001t0001g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(95): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(20): Show |
1 | a0001c0001t0001g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-13-1832_-13-1806d others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(53): Show |
1 | a0001c0001t0001g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(62): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(909): Show |
1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(918): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(59): Show |
1 | a0001c0001t0001g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(68): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(86): Show |
1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(95): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | ATCTCTGT others(58): Show |
1 | a0001c0001t0001g0081 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-13-1806_-13-1805i others(67): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914737
|
A | G | 31 | a0000c0003t0001g0033a0000c0003t0003g0238a0001c0001t0001g0010others(28): Show | 34 | HG00738.hp2 HG01070.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.-13-1805T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914737 | ||||||
chr19:41914740
|
TCTGTCTC others(14): Show |
T | 3 | a0000c0003t0003g0279a0001c0001t0003g0270a0001c0001t0003g0278 | 3 | HG00621.hp1 NA18993.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-13-1829_-13-1809d others(23): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914740 | ||||||
chr19:41914740
|
TCTGTCTC others(41): Show |
T | 1 | a0001c0001t0003g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-13-1856_-13-1809d others(50): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914740 | ||||||
chr19:41914740
|
TCTGTCTC others(114): Show |
T | 1 | a0001c0002t0002g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-13-1929_-13-1809d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914740 | ||||||
chr19:41914742
|
TGTCTCTC others(89): Show |
T | 2 | a0001c0001t0001g0106a0001c0002t0002g0148 | 2 | HG03688.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-13-1906_-13-1811d others(98): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914742 | ||||||
chr19:41914743
|
GTCTCTCC others(114): Show |
G | 1 | a0001c0001t0001g0204 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-13-1932_-13-1812d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914743 | ||||||
chr19:41914745
|
C | G | 1 | a0001c0002t0002g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13-1813G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914745 | ||||||
chr19:41914747
|
C | A | 5 | a0001c0001t0001g0191a0001c0001t0003g0245a0001c0001t0003g0250others(2): Show | 5 | HG00408.hp2 HG02083.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1815G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914747 | ||||||
chr19:41914747
|
C | CCGTCTT | 3 | a0001c0001t0003g0229a0001c0002t0002g0150a0001c0002t0002g0190 | 3 | HG02886.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-13-1816_-13-1815i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914747 | ||||||
chr19:41914747
|
C | CTCCCTCC others(26): Show |
1 | a0001c0001t0001g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-13-1816_-13-1815i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914747 | ||||||
chr19:41914747
|
C | CTGTCTA | 6 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0003g0249others(3): Show | 6 | HG01099.hp1 NA18970.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-1816_-13-1815i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914747 | ||||||
chr19:41914749
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1817G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914749 | ||||||
chr19:41914750
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1818G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914750 | ||||||
chr19:41914752
|
T | C | 3 | a0001c0002t0002g0121a0001c0004t0002g0035a0001c0004t0002g0036 | 3 | HG02055.hp2 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-1820A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914752 | ||||||
chr19:41914754
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1822G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914754 | ||||||
chr19:41914755
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-13-1823G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914755 | ||||||
chr19:41914756
|
C | T | 16 | a0000c0003t0001g0110a0000c0003t0001g0167a0001c0001t0001g0046others(13): Show | 16 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-13-1824G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914756 | ||||||
chr19:41914757
|
T | C | 57 | a0000c0003t0003g0238a0000c0003t0003g0248a0001c0001t0001g0011others(54): Show | 66 | HG00423.hp2 HG00544.hp1 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.-13-1825A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914757 | ||||||
chr19:41914757
|
T | TTCCACCA others(86): Show |
1 | a0001c0001t0001g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-13-1826_-13-1825i others(95): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914757 | ||||||
chr19:41914757
|
TTCCACCG others(93): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-13-1925_-13-1826d others(102): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914757 | ||||||
chr19:41914758
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0003g0232 | 2 | HG00642.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-13-1826A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914758 | ||||||
chr19:41914761
|
A | ACCATCT | 6 | a0000c0003t0003g0248a0001c0001t0001g0103a0001c0001t0001g0155others(3): Show | 7 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1830_-13-1829i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914761 | ||||||
chr19:41914761
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1829T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914761 | ||||||
chr19:41914761
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0003g0232 | 2 | HG00642.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-13-1829T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914761 | ||||||
chr19:41914762
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-13-1830G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914762 | ||||||
chr19:41914763
|
C | CATCTCCG others(32): Show |
1 | a0001c0001t0003g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-13-1832_-13-1831i others(41): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914763 | ||||||
chr19:41914763
|
C | CATCTCT | 14 | a0001c0001t0001g0054a0001c0001t0001g0085a0001c0001t0001g0177others(11): Show | 15 | HG00621.hp2 HG00738.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13-1832_-13-1831i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914763 | ||||||
chr19:41914763
|
C | CATCTCTG others(146): Show |
1 | a0002c0010t0001g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-13-1832_-13-1831i others(155): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914763 | ||||||
chr19:41914763
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-13-1831G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914763 | ||||||
chr19:41914763
|
CGTCTCT | C | 47 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0102others(44): Show | 55 | HG01109.hp2 HG01258.hp1 HG01261.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13-1837_-13-1832d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914763 | ||||||
chr19:41914763
|
CGTCTCTG others(125): Show |
C | 1 | a0001c0001t0003g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-13-1963_-13-1832d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914763 | ||||||
chr19:41914764
|
G | A | 29 | a0000c0003t0001g0110a0000c0003t0003g0238a0001c0001t0001g0046others(26): Show | 29 | HG00609.hp1 HG00738.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.-13-1832C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914764 | ||||||
chr19:41914764
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1832C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914764 | ||||||
chr19:41914765
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1833A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914765 | ||||||
chr19:41914767
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-13-1835A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914767 | ||||||
chr19:41914769
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01515.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-13-1837A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914769 | ||||||
chr19:41914769
|
TGTCTCTC others(62): Show |
T | 2 | a0001c0001t0003g0233a0001c0002t0002g0196 | 2 | HG01884.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-13-1906_-13-1838d others(71): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914769 | ||||||
chr19:41914772
|
C | G | 48 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0102others(45): Show | 56 | HG01109.hp2 HG01258.hp1 HG01261.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13-1840G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914772 | ||||||
chr19:41914774
|
C | A | 14 | a0000c0003t0003g0248a0000c0003t0003g0279a0001c0001t0001g0032others(11): Show | 14 | HG00544.hp1 HG00738.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13-1842G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914774 | ||||||
chr19:41914777
|
C | G | 1 | a0001c0001t0008g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-13-1845G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914777 | ||||||
chr19:41914779
|
T | C | 47 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0102others(44): Show | 55 | HG01109.hp2 HG01258.hp1 HG01261.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13-1847A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914779 | ||||||
chr19:41914782
|
C | T | 3 | a0001c0001t0003g0231a0001c0002t0002g0015a0004c0007t0001g0045 | 4 | HG01952.hp2 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-1850G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914782 | ||||||
chr19:41914783
|
C | T | 52 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0102others(49): Show | 60 | HG01109.hp2 HG01258.hp1 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.-13-1851G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914783 | ||||||
chr19:41914783
|
CT | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0169a0001c0001t0003g0245 | 3 | HG02083.hp1 NA18971.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-1852delA | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914783 | ||||||
chr19:41914784
|
T | C | 15 | a0000c0003t0001g0167a0001c0001t0001g0010a0001c0001t0001g0176others(12): Show | 16 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.-13-1852A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914784 | ||||||
chr19:41914785
|
T | C | 1 | a0000c0003t0003g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-13-1853A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914785 | ||||||
chr19:41914788
|
A | ACCATCT | 7 | a0001c0001t0001g0191a0001c0001t0003g0219a0001c0001t0003g0249others(4): Show | 7 | HG00408.hp2 HG00621.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1857_-13-1856i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914788 | ||||||
chr19:41914788
|
A | T | 1 | a0000c0003t0003g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-13-1856T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914788 | ||||||
chr19:41914789
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0169a0001c0001t0003g0245 | 3 | HG02083.hp1 NA18971.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-1857G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914789 | ||||||
chr19:41914790
|
C | CATCTCT | 4 | a0001c0001t0001g0188a0001c0001t0003g0232a0001c0001t0003g0263others(1): Show | 4 | HG00423.hp2 HG00642.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1859_-13-1858i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914790 | ||||||
chr19:41914790
|
C | T | 2 | a0001c0001t0003g0231a0001c0002t0002g0015 | 3 | HG01952.hp2 HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-13-1858G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914790 | ||||||
chr19:41914790
|
CGTCTCTG others(98): Show |
C | 2 | a0001c0001t0001g0136a0001c0001t0003g0259 | 2 | HG02559.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-13-1963_-13-1859d others(2): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914790 | ||||||
chr19:41914791
|
G | A | 44 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0003g0248others(41): Show | 45 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-13-1859C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914791 | ||||||
chr19:41914791
|
G | GTCTCTGT others(272): Show |
1 | a0001c0001t0001g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-13-1860_-13-1859i others(281): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914791 | ||||||
chr19:41914791
|
GTCTCTGT others(66): Show |
G | 2 | a0001c0001t0001g0032a0001c0001t0001g0152 | 2 | HG02074.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-13-1932_-13-1860d others(75): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914791 | ||||||
chr19:41914796
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0169a0001c0001t0001g0188 | 3 | NA18971.hp1 NA18989.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-1864A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914796 | ||||||
chr19:41914796
|
TGTCTCTC others(35): Show |
T | 4 | a0000c0003t0003g0248a0001c0001t0001g0103a0001c0001t0001g0195others(1): Show | 4 | HG00544.hp1 HG02055.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1906_-13-1865d others(44): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914796 | ||||||
chr19:41914797
|
GTCTCTCC others(60): Show |
G | 5 | a0000c0003t0001g0110a0000c0003t0003g0279a0001c0001t0003g0245others(2): Show | 5 | HG01975.hp2 HG02083.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1932_-13-1866d others(69): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914797 | ||||||
chr19:41914799
|
C | G | 1 | a0001c0001t0001g0010 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-1867G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914799 | ||||||
chr19:41914800
|
TCTCCCTC others(8): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-13-1883_-13-1869d others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914800 | ||||||
chr19:41914801
|
C | A | 1 | a0001c0001t0003g0277 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-13-1869G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914801 | ||||||
chr19:41914802
|
TCCCTCCC others(8): Show |
T | 10 | a0000c0003t0001g0167a0001c0001t0001g0101a0001c0001t0001g0169others(7): Show | 11 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13-1885_-13-1871d others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914802 | ||||||
chr19:41914804
|
CCT | C | 42 | a0001c0001t0001g0102a0001c0001t0003g0009a0001c0001t0003g0225others(39): Show | 49 | HG00558.hp2 HG01109.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.-13-1874_-13-1873d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914804 | ||||||
chr19:41914806
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049 | 5 | HG01258.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1874A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914806 | ||||||
chr19:41914806
|
TCCCCCTC others(39): Show |
T | 1 | a0001c0002t0002g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-13-1920_-13-1875d others(48): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914806 | ||||||
chr19:41914809
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-13-1877G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914809 | ||||||
chr19:41914809
|
CCCTCCAC others(16): Show |
C | 2 | a0001c0001t0001g0011a0001c0001t0001g0049 | 3 | HG01258.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-13-1900_-13-1878d others(25): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914809 | ||||||
chr19:41914810
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0177a0001c0001t0001g0188others(1): Show | 5 | HG00642.hp1 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1878G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914810 | ||||||
chr19:41914811
|
C | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0177a0001c0001t0001g0179others(16): Show | 20 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-13-1879G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914811 | ||||||
chr19:41914816
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-13-1884G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914816 | ||||||
chr19:41914816
|
CCGTGTCT others(65): Show |
C | 1 | a0001c0001t0003g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-13-1956_-13-1885d others(74): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914816 | ||||||
chr19:41914817
|
C | CATCTCCG others(5): Show |
3 | a0001c0001t0001g0182a0001c0001t0003g0222a0001c0001t0003g0253 | 3 | HG02083.hp2 HG02155.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-13-1886_-13-1885i others(14): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
C | CATCTCCG others(38): Show |
1 | a0001c0001t0003g0263 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-13-1886_-13-1885i others(47): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
C | CATCTCT | 7 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0003g0223others(4): Show | 7 | HG00642.hp1 HG03492.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-1886_-13-1885i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
C | CATCTCTG others(5): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0179 | 2 | NA19083.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-13-1886_-13-1885i others(14): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
C | CATCTCTG others(229): Show |
1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-13-1886_-13-1885i others(238): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
C | CGTCTCT | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0002t0002g0116 | 3 | HG02886.hp2 NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-13-1886_-13-1885i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-13-1885G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914817
|
CGTGTCTC others(71): Show |
C | 2 | a0001c0001t0003g0277a0001c0001t0014g0282 | 2 | NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-13-1963_-13-1886d others(80): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914817 | ||||||
chr19:41914818
|
G | A | 57 | a0001c0001t0001g0191a0001c0001t0003g0009a0001c0001t0003g0218others(54): Show | 64 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-13-1886C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914818 | ||||||
chr19:41914819
|
TGTCTCCC others(8): Show |
T | 9 | a0001c0001t0003g0219a0001c0001t0003g0249a0001c0001t0003g0250others(6): Show | 9 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13-1902_-13-1888d others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914819 | ||||||
chr19:41914819
|
TGTCTCCC others(33): Show |
T | 2 | a0001c0001t0003g0231a0001c0001t0003g0244 | 2 | HG01952.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-13-1927_-13-1888d others(42): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914819 | ||||||
chr19:41914820
|
G | C | 78 | a0000c0003t0001g0167a0001c0001t0001g0101a0001c0001t0001g0102others(75): Show | 86 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-13-1888C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914820 | ||||||
chr19:41914822
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-13-1890G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914822 | ||||||
chr19:41914823
|
TCCCCCCC others(8): Show |
T | 48 | a0001c0001t0001g0191a0001c0001t0003g0009a0001c0001t0003g0218others(45): Show | 55 | HG00423.hp2 HG00621.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.-13-1906_-13-1892d others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914823 | ||||||
chr19:41914825
|
C | G | 3 | a0000c0003t0001g0167a0001c0001t0001g0102a0001c0001t0001g0168 | 3 | HG00597.hp1 NA18944.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-13-1893G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914825 | ||||||
chr19:41914825
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-1893G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914825 | ||||||
chr19:41914827
|
C | T | 32 | a0000c0003t0001g0167a0000c0003t0003g0238a0001c0001t0001g0101others(29): Show | 33 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-13-1895G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914827 | ||||||
chr19:41914830
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-13-1898G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914830 | ||||||
chr19:41914831
|
T | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0155a0001c0001t0001g0177others(17): Show | 21 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13-1899A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914831 | ||||||
chr19:41914832
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0177a0001c0001t0001g0182others(3): Show | 7 | HG00738.hp1 HG01515.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-1900A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914832 | ||||||
chr19:41914836
|
A | T | 9 | a0001c0001t0003g0219a0001c0001t0003g0249a0001c0001t0003g0250others(6): Show | 9 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13-1904T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914836 | ||||||
chr19:41914838
|
C | CATCTCT | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0003g0257others(3): Show | 6 | HG00738.hp1 HG02886.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1907_-13-1906i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914838 | ||||||
chr19:41914839
|
G | A | 23 | a0000c0003t0001g0167a0000c0003t0003g0238a0001c0001t0001g0010others(20): Show | 26 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-13-1907C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914839 | ||||||
chr19:41914845
|
GTCTCTCC others(12): Show |
G | 1 | a0001c0001t0003g0273 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-13-1932_-13-1914d others(21): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914845 | ||||||
chr19:41914849
|
C | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0105others(10): Show | 15 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-1917G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914849 | ||||||
chr19:41914850
|
T | TGTCTCTC others(1): Show |
3 | a0001c0001t0003g0274a0001c0001t0003g0275a0001c0001t0003g0281 | 3 | NA18973.hp1 NA19004.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-13-1919_-13-1918i others(10): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914850 | ||||||
chr19:41914852
|
C | CCT | 31 | a0000c0003t0003g0248a0001c0001t0001g0008a0001c0001t0001g0103others(28): Show | 33 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.-13-1921_-13-1920i others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914852 | ||||||
chr19:41914852
|
C | G | 80 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0142others(77): Show | 103 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-13-1920G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914852 | ||||||
chr19:41914852
|
C | T | 4 | a0001c0001t0003g0232a0001c0001t0003g0274a0001c0001t0003g0275others(1): Show | 4 | HG00642.hp1 NA18973.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-1920G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914852 | ||||||
chr19:41914853
|
CCCCCTCC others(19): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-1947_-13-1922d others(28): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914853 | ||||||
chr19:41914854
|
C | T | 110 | a0000c0003t0001g0167a0000c0003t0003g0238a0000c0005t0002g0099others(107): Show | 138 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.-13-1922G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914854 | ||||||
chr19:41914855
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-13-1923G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914855 | ||||||
chr19:41914856
|
C | T | 1 | a0001c0002t0002g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-13-1924G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914856 | ||||||
chr19:41914857
|
C | CCTCCACC others(192): Show |
1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-13-1926_-13-1925i others(201): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | CCTTCCAC others(82): Show |
1 | a0001c0001t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-13-1926_-13-1925i others(91): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | CTCCACCA others(191): Show |
1 | a0001c0001t0001g0048 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-13-1926_-13-1925i others(200): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | CTCCACCA others(191): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0046 | 3 | NA18945.hp2 NA18965.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-13-1926_-13-1925i others(200): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | CTCCACCA others(52): Show |
1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13-1926_-13-1925i others(61): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | CTCCACCA others(26): Show |
12 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0003g0229others(9): Show | 13 | HG00738.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-13-1926_-13-1925i others(35): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | CTT | 108 | a0000c0003t0001g0167a0000c0003t0003g0238a0000c0005t0002g0099others(105): Show | 136 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.-13-1926_-13-1925i others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914857
|
C | T | 33 | a0000c0003t0003g0248a0001c0001t0001g0008a0001c0001t0001g0103others(30): Show | 35 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.-13-1925G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914857 | ||||||
chr19:41914861
|
A | T | 2 | a0001c0001t0003g0231a0001c0001t0003g0244 | 2 | HG01952.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-13-1929T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914861 | ||||||
chr19:41914862
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-13-1930G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914862 | ||||||
chr19:41914862
|
CCATCTCT others(19): Show |
C | 2 | a0001c0001t0001g0041a0001c0002t0002g0091 | 2 | HG02818.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-13-1956_-13-1931d others(28): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914862 | ||||||
chr19:41914863
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-13-1931G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914863 | ||||||
chr19:41914863
|
CATCTCTG others(25): Show |
C | 1 | a0000c0003t0003g0248 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-13-1963_-13-1932d others(34): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914863 | ||||||
chr19:41914864
|
A | ATCTCCG | 3 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0003g0249 | 3 | HG02083.hp2 NA19079.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-13-1933_-13-1932i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914864 | ||||||
chr19:41914864
|
A | ATCTCTGT others(194): Show |
1 | a0001c0001t0001g0055 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-13-1933_-13-1932i others(203): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914864 | ||||||
chr19:41914864
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0186others(6): Show | 11 | HG00642.hp1 HG00642.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-1932T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914864 | ||||||
chr19:41914874
|
C | A | 5 | a0000c0003t0001g0110a0001c0001t0001g0182a0001c0001t0003g0249others(2): Show | 5 | HG01975.hp2 HG02083.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1942G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914874 | ||||||
chr19:41914874
|
C | CTGTCTA | 6 | a0001c0001t0001g0155a0001c0001t0003g0223a0001c0001t0003g0256others(3): Show | 6 | HG00280.hp1 HG01884.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1943_-13-1942i others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914874 | ||||||
chr19:41914876
|
C | G | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0221others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1944G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914876 | ||||||
chr19:41914877
|
C | T | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0221others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1945G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914877 | ||||||
chr19:41914879
|
T | TC | 6 | a0001c0001t0001g0175a0001c0001t0001g0204a0001c0001t0003g0222others(3): Show | 6 | HG00609.hp1 HG00642.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1948dupG | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914879 | ||||||
chr19:41914879
|
TC | T | 6 | a0001c0002t0002g0020a0001c0002t0002g0022a0001c0002t0002g0122others(3): Show | 8 | HG00544.hp2 HG02165.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-1948delG | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914879 | ||||||
chr19:41914880
|
C | CT | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0221others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1949_-13-1948i others(3): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914880 | ||||||
chr19:41914882
|
C | G | 3 | a0001c0002t0002g0135a0001c0004t0002g0035a0001c0004t0002g0036 | 3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-1950G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914882 | ||||||
chr19:41914882
|
C | T | 1 | a0001c0001t0003g0244 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-13-1950G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914882 | ||||||
chr19:41914883
|
C | CT | 8 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0003g0220others(5): Show | 8 | HG00738.hp1 HG02083.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-1952dupA | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914883 | ||||||
chr19:41914883
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | NA19000.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-13-1951G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914883 | ||||||
chr19:41914885
|
C | T | 16 | a0000c0003t0001g0110a0000c0003t0003g0279a0001c0001t0001g0155others(13): Show | 16 | HG00280.hp1 HG00423.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-13-1953G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914885 | ||||||
chr19:41914886
|
CATCAT | C | 16 | a0000c0003t0001g0110a0000c0003t0003g0279a0001c0001t0001g0155others(13): Show | 16 | HG00280.hp1 HG00423.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-13-1959_-13-1955d others(7): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914886 | ||||||
chr19:41914887
|
A | C | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0221others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1955T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914887 | ||||||
chr19:41914888
|
T | C | 25 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0184others(22): Show | 25 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13-1956A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914888 | ||||||
chr19:41914889
|
C | T | 14 | a0001c0001t0001g0186a0001c0001t0003g0218a0001c0001t0003g0219others(11): Show | 14 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13-1957G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914889 | ||||||
chr19:41914890
|
A | T | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0221others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1958T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914890 | ||||||
chr19:41914891
|
T | C | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0221others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13-1959A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914891 | ||||||
chr19:41914893
|
T | A | 29 | a0000c0003t0001g0110a0000c0003t0003g0279a0001c0001t0001g0155others(26): Show | 29 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.-13-1961A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914893 | ||||||
chr19:41914895
|
T | C | 166 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0001g0170others(163): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-13-1963A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914895 | ||||||
chr19:41914895
|
T | TGTCTCTG others(20): Show |
4 | a0001c0001t0001g0179a0001c0001t0003g0257a0001c0001t0003g0263others(1): Show | 4 | HG00738.hp1 HG03492.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-1964_-13-1963i others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914895 | ||||||
chr19:41914895
|
T | TGTCTCTG others(20): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0003g0249 | 3 | HG02083.hp2 NA18981.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-13-1964_-13-1963i others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914895 | ||||||
chr19:41914896
|
G | A | 3 | a0001c0002t0002g0135a0001c0004t0002g0035a0001c0004t0002g0036 | 3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-1964C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914896 | ||||||
chr19:41914906
|
C | A | 2 | a0001c0001t0003g0228a0001c0002t0009g0159 | 2 | HG03834.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-13-1974G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914906 | ||||||
chr19:41914914
|
C | T | 2 | a0001c0001t0003g0231a0001c0001t0003g0232 | 2 | HG00642.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-13-1982G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914914 | ||||||
chr19:41914916
|
C | T | 3 | a0001c0001t0003g0228a0001c0001t0003g0231a0001c0001t0003g0232 | 3 | HG00642.hp1 HG01952.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-13-1984G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914916 | ||||||
chr19:41914922
|
C | T | 2 | a0001c0001t0003g0231a0001c0001t0003g0232 | 2 | HG00642.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-13-1990G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914922 | ||||||
chr19:41914923
|
A | ATCTCCGT others(86): Show |
1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-13-1992_-13-1991i others(95): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914923 | ||||||
chr19:41914923
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-13-1991T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914923 | ||||||
chr19:41914929
|
G | GTCTCTGT others(20): Show |
2 | a0001c0001t0003g0222a0001c0001t0003g0224 | 2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-13-2024_-13-1998d others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914929 | ||||||
chr19:41914947
|
T | C | 1 | a0001c0002t0002g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-13-2015A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914947 | ||||||
chr19:41914955
|
T | C | 2 | a0001c0001t0001g0176a0001c0002t0002g0160 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-13-2023A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914955 | ||||||
chr19:41914956
|
A | ATCTCTGT others(91): Show |
2 | a0001c0002t0002g0127a0006c0012t0002g0126 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-2025_-13-2024i others(100): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914956 | ||||||
chr19:41914966
|
C | CTG | 130 | a0000c0003t0001g0167a0000c0003t0001g0170a0000c0005t0002g0099others(127): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-13-2035_-13-2034i others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914966 | ||||||
chr19:41914969
|
C | CCTCCTCT others(22): Show |
2 | a0001c0002t0002g0127a0006c0012t0002g0126 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-2038_-13-2037i others(31): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914969 | ||||||
chr19:41914969
|
C | T | 130 | a0000c0003t0001g0167a0000c0003t0001g0170a0000c0005t0002g0099others(127): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-13-2037G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41914969 | ||||||
chr19:41915032
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-13-2100C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915032 | ||||||
chr19:41915131
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-13-2199G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915131 | ||||||
chr19:41915132
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-13-2200C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915132 | ||||||
chr19:41915347
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-2415G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915347 | ||||||
chr19:41915380
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-13-2448C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915380 | ||||||
chr19:41915399
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-13-2467G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915399 | ||||||
chr19:41915412
|
G | A | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-2480C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915412 | ||||||
chr19:41915472
|
TTCTGTGT others(9): Show |
T | 1 | a0001c0002t0002g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13-2556_-13-2541d others(18): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915472 | ||||||
chr19:41915485
|
C | T | 82 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(79): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-13-2553G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915485 | ||||||
chr19:41915543
|
C | T | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-2611G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915543 | ||||||
chr19:41915654
|
T | C | 1 | a0001c0001t0003g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13-2722A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915654 | ||||||
chr19:41915729
|
G | A | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-2797C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915729 | ||||||
chr19:41915804
|
T | C | 1 | a0001c0002t0002g0147 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-13-2872A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915804 | ||||||
chr19:41915817
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-13-2885C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915817 | ||||||
chr19:41915818
|
C | T | 1 | a0001c0001t0012g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13-2886G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915818 | ||||||
chr19:41915865
|
C | T | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-2933G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915865 | ||||||
chr19:41915913
|
G | A | 1 | a0001c0002t0002g0147 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-13-2981C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915913 | ||||||
chr19:41915932
|
A | C | 1 | a0001c0002t0002g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-13-3000T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915932 | ||||||
chr19:41915932
|
A | G | 96 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(93): Show | 121 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.-13-3000T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915932 | ||||||
chr19:41915939
|
T | C | 1 | a0001c0001t0003g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-13-3007A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915939 | ||||||
chr19:41915941
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13-3009G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41915941 | ||||||
chr19:41916021
|
C | A | 2 | a0001c0002t0002g0115a0001c0002t0002g0116 | 2 | HG00738.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-13-3089G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916021 | ||||||
chr19:41916022
|
CT | C | 3 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092 | 3 | HG02818.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-13-3091delA | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916022 | ||||||
chr19:41916025
|
C | T | 2 | a0001c0004t0005g0211a0001c0004t0005g0212 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-13-3093G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916025 | ||||||
chr19:41916214
|
A | T | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-3282T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916214 | ||||||
chr19:41916281
|
CAA | C | 96 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(93): Show | 121 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.-13-3351_-13-3350d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916281 | ||||||
chr19:41916656
|
A | G | 2 | a0001c0001t0003g0002a0001c0001t0003g0226 | 6 | HG01106.hp2 HG01515.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-3724T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916656 | ||||||
chr19:41916720
|
C | T | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-3788G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916720 | ||||||
chr19:41916838
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-13-3906G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916838 | ||||||
chr19:41916843
|
G | GAC | 99 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(96): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-13-3913_-13-3912d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916843 | ||||||
chr19:41916851
|
C | T | 1 | a0001c0001t0011g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-13-3919G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916851 | ||||||
chr19:41916895
|
G | T | 93 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(90): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13-3963C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916895 | ||||||
chr19:41916992
|
A | G | 99 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(96): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-13-4060T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41916992 | ||||||
chr19:41917011
|
T | TGC | 91 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(88): Show | 114 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-13-4080_-13-4079i others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917011 | ||||||
chr19:41917013
|
T | C | 8 | a0001c0001t0011g0214a0001c0001t0012g0215a0001c0004t0005g0026others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-4081A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917013 | ||||||
chr19:41917046
|
C | T | 6 | a0001c0002t0002g0015a0001c0002t0002g0031a0001c0002t0002g0111others(3): Show | 7 | HG02145.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4114G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917046 | ||||||
chr19:41917121
|
G | A | 1 | a0001c0002t0002g0003 | 4 | HG02257.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-4189C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917121 | ||||||
chr19:41917123
|
C | T | 282 | a0000c0003t0001g0033a0000c0003t0001g0088a0000c0003t0001g0110others(279): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-13-4191G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917123 | ||||||
chr19:41917407
|
C | T | 1 | a0001c0002t0002g0140 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-13-4475G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917407 | ||||||
chr19:41917432
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-13-4500C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917432 | ||||||
chr19:41917642
|
GCACA | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0086 | 3 | HG01346.hp2 HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-13-4714_-13-4711d others(6): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917642 | ||||||
chr19:41917652
|
G | A | 8 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0004t0005g0026others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-4720C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917652 | ||||||
chr19:41917695
|
G | A | 88 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(85): Show | 111 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-13-4763C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917695 | ||||||
chr19:41917710
|
G | A | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-4778C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917710 | ||||||
chr19:41917737
|
G | A | 7 | a0000c0005t0002g0119a0001c0004t0005g0026a0001c0004t0005g0027others(4): Show | 9 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13-4805C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917737 | ||||||
chr19:41917763
|
CAGT | C | 6 | a0001c0002t0002g0023a0001c0002t0002g0039a0001c0002t0002g0040others(3): Show | 7 | HG00438.hp2 NA18747.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4834_-13-4832d others(5): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917763 | ||||||
chr19:41917861
|
C | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0183a0001c0001t0001g0184 | 4 | HG02027.hp1 NA18981.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-4929G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917861 | ||||||
chr19:41917937
|
T | C | 93 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(90): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13-5005A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41917937 | ||||||
chr19:41918097
|
T | C | 90 | a0000c0005t0002g0119a0001c0001t0001g0136a0001c0001t0001g0142others(87): Show | 113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-13-5165A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918097 | ||||||
chr19:41918184
|
C | T | 93 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(90): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13-5252G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918184 | ||||||
chr19:41918197
|
T | C | 99 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(96): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-13-5265A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918197 | ||||||
chr19:41918391
|
T | C | 2 | a0001c0002t0002g0017a0001c0002t0002g0139 | 3 | HG02451.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-13-5459A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918391 | ||||||
chr19:41918416
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-13-5484G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918416 | ||||||
chr19:41918424
|
T | TCA | 93 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(90): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13-5494_-13-5493d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918424 | ||||||
chr19:41918481
|
C | T | 1 | a0001c0002t0002g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13-5549G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918481 | ||||||
chr19:41918493
|
ACAC | A | 3 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202 | 3 | HG01109.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-13-5564_-13-5562d others(5): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918493 | ||||||
chr19:41918498
|
T | C | 1 | a0001c0001t0012g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13-5566A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918498 | ||||||
chr19:41918509
|
CCA | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049 | 5 | HG01258.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5579_-13-5578d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918509 | ||||||
chr19:41918516
|
C | T | 1 | a0001c0001t0012g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13-5584G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918516 | ||||||
chr19:41918616
|
ACAC | A | 6 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-5687_-13-5685d others(5): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918616 | ||||||
chr19:41918725
|
A | T | 3 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0213 | 5 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-5793T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918725 | ||||||
chr19:41918760
|
TACATCTA others(7): Show |
T | 1 | a0001c0001t0003g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-13-5842_-13-5829d others(16): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918760 | ||||||
chr19:41918970
|
C | CCA | 6 | a0000c0005t0002g0099a0001c0002t0002g0090a0001c0002t0002g0091others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-6040_-13-6039d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41918970 | ||||||
chr19:41919017
|
C | G | 2 | a0001c0002t0002g0198a0001c0002t0002g0199 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-13-6085G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919017 | ||||||
chr19:41919020
|
G | A | 98 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(95): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-13-6088C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919020 | ||||||
chr19:41919067
|
C | T | 91 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(88): Show | 114 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-13-6135G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919067 | ||||||
chr19:41919103
|
T | C | 99 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(96): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-13-6171A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919103 | ||||||
chr19:41919153
|
A | T | 92 | a0000c0005t0002g0119a0001c0001t0001g0136a0001c0001t0001g0142others(89): Show | 115 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-13-6221T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919153 | ||||||
chr19:41919154
|
C | T | 1 | a0000c0005t0002g0099 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-13-6222G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919154 | ||||||
chr19:41919159
|
C | T | 1 | a0001c0004t0005g0026 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-6227G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919159 | ||||||
chr19:41919313
|
A | C | 1 | a0001c0001t0003g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-13-6381T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919313 | ||||||
chr19:41919323
|
G | C | 99 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(96): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-13-6391C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919323 | ||||||
chr19:41919426
|
C | T | 2 | a0001c0002t0002g0127a0006c0012t0002g0126 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13-6494G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919426 | ||||||
chr19:41919494
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-13-6562G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919494 | ||||||
chr19:41919512
|
T | TAC | 63 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0102others(60): Show | 77 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-13-6582_-13-6581d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919512 | ||||||
chr19:41919512
|
T | TACAC | 44 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0142others(41): Show | 53 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-13-6584_-13-6581d others(6): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919512 | ||||||
chr19:41919512
|
T | TACACAC | 7 | a0001c0002t0002g0092a0001c0002t0002g0149a0001c0004t0005g0026others(4): Show | 9 | HG01891.hp2 HG02109.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13-6586_-13-6581d others(8): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919512 | ||||||
chr19:41919512
|
TAC | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG02027.hp2 HG04228.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13-6582_-13-6581d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919512 | ||||||
chr19:41919599
|
C | T | 100 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(97): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-13-6667G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919599 | ||||||
chr19:41919645
|
C | T | 3 | a0000c0003t0015g0283a0001c0001t0003g0006a0001c0001t0003g0224 | 6 | HG01943.hp1 HG01978.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-6713G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919645 | ||||||
chr19:41919742
|
T | A | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13-6810A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919742 | ||||||
chr19:41919791
|
T | TAAG | 98 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(95): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-13-6860_-13-6859i others(5): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919791 | ||||||
chr19:41919815
|
T | C | 98 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(95): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-13-6883A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919815 | ||||||
chr19:41919836
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-13-6904C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919836 | ||||||
chr19:41919914
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-13-6982G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919914 | ||||||
chr19:41919943
|
G | A | 2 | a0000c0003t0003g0279a0001c0001t0003g0278 | 2 | NA18993.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-13-7011C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919943 | ||||||
chr19:41919955
|
C | T | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-7023G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41919955 | ||||||
chr19:41920007
|
ACTCACAG others(10): Show |
A | 1 | a0001c0002t0002g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-13-7092_-13-7076d others(19): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920007 | ||||||
chr19:41920075
|
T | A | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-7143A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920075 | ||||||
chr19:41920104
|
A | G | 98 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(95): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-13-7172T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920104 | ||||||
chr19:41920167
|
T | TCA | 94 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(91): Show | 117 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-13-7237_-13-7236d others(4): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920167 | ||||||
chr19:41920193
|
C | T | 1 | a0003c0006t0002g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-13-7261G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920193 | ||||||
chr19:41920195
|
C | T | 1 | a0001c0001t0011g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-13-7263G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920195 | ||||||
chr19:41920237
|
G | A | 4 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092others(1): Show | 4 | HG02818.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-7305C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920237 | ||||||
chr19:41920285
|
G | A | 86 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(83): Show | 109 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-13-7353C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920285 | ||||||
chr19:41920299
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-13-7367C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920299 | ||||||
chr19:41920343
|
TGCACTCA others(8): Show |
T | 1 | a0001c0001t0012g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13-7426_-13-7412d others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920343 | ||||||
chr19:41920358
|
C | T | 88 | a0000c0005t0002g0099a0000c0005t0002g0119a0001c0001t0001g0136others(85): Show | 111 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-13-7426G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920358 | ||||||
chr19:41920367
|
A | G | 1 | a0001c0004t0005g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-13-7435T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920367 | ||||||
chr19:41920423
|
A | G | 9 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092others(6): Show | 11 | HG01891.hp2 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-7491T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920423 | ||||||
chr19:41920427
|
A | ACAGACAT others(70): Show |
3 | a0001c0002t0002g0007a0001c0002t0002g0198a0001c0002t0002g0199 | 5 | HG02257.hp2 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+7536_-13-7496d others(79): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920427 | ||||||
chr19:41920482
|
G | C | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-7550C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920482 | ||||||
chr19:41920485
|
A | ACACACAG others(8): Show |
1 | a0001c0001t0001g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14+7540_-14+7554d others(17): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920485 | ||||||
chr19:41920843
|
G | A | 1 | a0001c0002t0002g0022 | 2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-14+7197C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920843 | ||||||
chr19:41920902
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14+7138G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920902 | ||||||
chr19:41920942
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA19058.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-14+7098G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920942 | ||||||
chr19:41920997
|
G | A | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+7043C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920997 | ||||||
chr19:41920998
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-14+7042G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41920998 | ||||||
chr19:41921000
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-14+7040G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921000 | ||||||
chr19:41921028
|
G | A | 3 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0213 | 5 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+7012C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921028 | ||||||
chr19:41921057
|
G | A | 2 | a0001c0004t0002g0035a0001c0004t0002g0036 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-14+6983C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921057 | ||||||
chr19:41921070
|
C | T | 1 | a0001c0002t0002g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-14+6970G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921070 | ||||||
chr19:41921102
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-14+6938G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921102 | ||||||
chr19:41921189
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-14+6851T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921189 | ||||||
chr19:41921319
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | NA18964.hp1 NA19004.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+6721A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921319 | ||||||
chr19:41921374
|
C | T | 1 | a0001c0002t0004g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-14+6666G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921374 | ||||||
chr19:41921484
|
A | G | 3 | a0001c0001t0012g0215a0001c0004t0005g0211a0001c0004t0005g0212 | 3 | HG03195.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-14+6556T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921484 | ||||||
chr19:41921529
|
CCGAGGTG others(20): Show |
C | 3 | a0001c0002t0002g0007a0001c0002t0002g0198a0001c0002t0002g0199 | 5 | HG02257.hp2 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+6484_-14+6510d others(29): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921529 | ||||||
chr19:41921557
|
C | T | 1 | a0000c0005t0002g0119 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14+6483G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921557 | ||||||
chr19:41921734
|
G | T | 1 | a0001c0002t0004g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-14+6306C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921734 | ||||||
chr19:41921847
|
C | T | 2 | a0001c0002t0002g0200a0001c0002t0002g0201 | 2 | HG01109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-14+6193G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41921847 | ||||||
chr19:41922093
|
C | T | 83 | a0000c0005t0002g0119a0001c0001t0001g0136a0001c0001t0001g0142others(80): Show | 107 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.-14+5947G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922093 | ||||||
chr19:41922196
|
G | A | 1 | a0001c0004t0005g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-14+5844C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922196 | ||||||
chr19:41922222
|
G | A | 1 | a0001c0001t0003g0280 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-14+5818C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922222 | ||||||
chr19:41922453
|
G | A | 3 | a0001c0002t0002g0109a0001c0002t0002g0193a0001c0002t0002g0194 | 3 | HG02486.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-14+5587C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922453 | ||||||
chr19:41922464
|
C | T | 1 | a0001c0001t0003g0222 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-14+5576G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922464 | ||||||
chr19:41922518
|
G | C | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+5522C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922518 | ||||||
chr19:41922711
|
C | T | 9 | a0001c0002t0002g0015a0001c0002t0002g0031a0001c0002t0002g0111others(6): Show | 10 | HG00738.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14+5329G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41922711 | ||||||
chr19:41923229
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-14+4811A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923229 | ||||||
chr19:41923318
|
A | C | 1 | a0001c0002t0002g0205 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14+4722T>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923318 | ||||||
chr19:41923536
|
T | C | 282 | a0000c0003t0001g0033a0000c0003t0001g0088a0000c0003t0001g0110others(279): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-14+4504A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923536 | ||||||
chr19:41923647
|
C | A | 8 | a0001c0002t0002g0001a0001c0002t0002g0025a0001c0002t0002g0196others(5): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14+4393G>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923647 | ||||||
chr19:41923675
|
T | TGTGTCTG others(476): Show |
1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-14+4364_-14+4365i others(485): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923675 | ||||||
chr19:41923734
|
G | A | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+4306C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923734 | ||||||
chr19:41923797
|
G | C | 204 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0001g0170others(201): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-14+4243C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923797 | ||||||
chr19:41923803
|
C | T | 1 | a0001c0001t0011g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14+4237G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923803 | ||||||
chr19:41923884
|
TGGTAGGG others(76): Show |
T | 4 | a0001c0002t0002g0015a0001c0002t0002g0031a0001c0002t0002g0111others(1): Show | 5 | HG02145.hp1 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+4073_-14+4155d others(85): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923884 | ||||||
chr19:41923902
|
A | AGGGGCTG others(40): Show |
2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02135.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-14+4091_-14+4137d others(49): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923902 | ||||||
chr19:41923937
|
G | A | 1 | a0000c0003t0001g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-14+4103C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923937 | ||||||
chr19:41923979
|
G | C | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+4061C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41923979 | ||||||
chr19:41924016
|
G | T | 1 | a0000c0003t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14+4024C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41924016 | ||||||
chr19:41924437
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14+3603G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41924437 | ||||||
chr19:41924576
|
G | GT | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+3463dupA | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41924576 | ||||||
chr19:41924612
|
G | A | 1 | a0001c0011t0007g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+3428C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41924612 | ||||||
chr19:41924615
|
A | G | 204 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0001g0170others(201): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-14+3425T>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41924615 | ||||||
chr19:41925001
|
C | T | 5 | a0001c0004t0005g0026a0001c0004t0005g0027a0001c0004t0005g0211others(2): Show | 7 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+3039G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925001 | ||||||
chr19:41925176
|
G | A | 3 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202 | 3 | HG01109.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-14+2864C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925176 | ||||||
chr19:41925223
|
G | T | 1 | a0001c0002t0002g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14+2817C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925223 | ||||||
chr19:41925396
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0203 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-14+2644A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925396 | ||||||
chr19:41925429
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0219 | 2 | HG00621.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-14+2611G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925429 | ||||||
chr19:41925479
|
G | A | 1 | a0001c0002t0004g0209 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14+2561C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925479 | ||||||
chr19:41925681
|
G | A | 204 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0001g0170others(201): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-14+2359C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925681 | ||||||
chr19:41925716
|
C | T | 2 | a0001c0004t0002g0035a0001c0004t0002g0036 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-14+2324G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925716 | ||||||
chr19:41925788
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-14+2252C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41925788 | ||||||
chr19:41926101
|
C | T | 4 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092others(1): Show | 4 | HG02818.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1939G>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926101 | ||||||
chr19:41926102
|
G | A | 4 | a0001c0002t0002g0001a0001c0002t0002g0025a0001c0002t0002g0205others(1): Show | 10 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+1938C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926102 | ||||||
chr19:41926122
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-14+1918C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926122 | ||||||
chr19:41926351
|
G | A | 2 | a0001c0002t0004g0208a0001c0002t0004g0209 | 2 | NA18965.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-14+1689C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926351 | ||||||
chr19:41926460
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-14+1580A>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926460 | ||||||
chr19:41926573
|
C | G | 1 | a0001c0002t0002g0107 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-14+1467G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926573 | ||||||
chr19:41926631
|
T | C | 6 | a0001c0001t0011g0214a0001c0001t0012g0215a0001c0002t0002g0090others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+1409A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926631 | ||||||
chr19:41926639
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-14+1401A>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926639 | ||||||
chr19:41926690
|
G | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG01070.hp1 HG01243.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+1350C>G | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926690 | ||||||
chr19:41926721
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-14+1319C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926721 | ||||||
chr19:41926728
|
C | CG | 11 | a0000c0003t0001g0033a0000c0005t0002g0099a0001c0001t0001g0034others(8): Show | 11 | HG01106.hp1 HG03654.hp1 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14+1311dupC | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926728 | ||||||
chr19:41926761
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-14+1279C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926761 | ||||||
chr19:41926881
|
G | A | 205 | a0000c0003t0001g0110a0000c0003t0001g0167a0000c0003t0001g0170others(202): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-14+1159C>T | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926881 | ||||||
chr19:41926956
|
GAGATAGA others(7): Show |
G | 1 | a0001c0001t0003g0281 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-14+1070_-14+1083d others(16): Show |
ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41926956 | ||||||
chr19:41927344
|
A | T | 2 | a0001c0004t0005g0026a0001c0004t0005g0027 | 4 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+696T>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41927344 | ||||||
chr19:41927421
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-14+619G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41927421 | ||||||
chr19:41927723
|
C | G | 1 | a0001c0002t0002g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14+317G>C | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41927723 | ||||||
chr19:41927833
|
G | T | 1 | a0001c0002t0002g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14+207C>A | ERFL | ENSG00000268041.3 | transcript | ENST00000597630.3 | protein_coding | 1/5 | chr19 | 41927833 |