geneid | 6059 |
---|---|
ensemblid | ENSG00000164163.11 |
hgncid | 69 |
symbol | ABCE1 |
name | ATP binding cassette subfamily E member 1 |
refseq_nuc | NM_002940.3 |
refseq_prot | NP_002931.2 |
ensembl_nuc | ENST00000296577.9 |
ensembl_prot | ENSP00000296577.4 |
mane_status | MANE Select |
chr | chr4 |
start | 145098311 |
end | 145129524 |
strand | + |
ver | v1.2 |
region | chr4:145098311-145129524 |
region5000 | chr4:145093311-145134524 |
regionname0 | ABCE1_chr4_145098311_145129524 |
regionname5000 | ABCE1_chr4_145093311_145134524 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 599 | 259 | 88 | 56 | 77 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0002 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1800 | 251 | 81 | 55 | 77 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
c0002 | 0/0 | 1800 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
c0003 | 0/0 | 1800 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
c0004 | 0/0 | 1800 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
c0005 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2088 | 243 | 75 | 54 | 76 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0002 | 0/0 | 2088 | 4 | 3 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0003 | 0/0 | 2088 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0004 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0005 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0006 | 0/0 | 2088 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0007 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0008 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
t0009 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 24 | 3 | 8 | 7 | 1 | 5 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0002 | 0/0 | 23 | 2 | 8 | 12 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0003 | 0/0 | 18 | 0 | 9 | 5 | 2 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0004 | 0/0 | 8 | 2 | 2 | 3 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0005 | 0/0 | 8 | 2 | 1 | 2 | 1 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0009 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0028 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/1 | 251 | 81 | 55 | 77 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0004 | a0001 | c0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0002c0005 | a0002 | c0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 242 | 75 | 54 | 75 | 10 | 26 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0003t0006 | a0001 | c0003 | t0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0001c0004t0004 | a0001 | c0004 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
a0002c0005t0001 | a0002 | c0005 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 23 | 3 | 8 | 6 | 1 | 5 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 23 | 2 | 8 | 12 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 18 | 0 | 9 | 5 | 2 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 8 | 2 | 2 | 3 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 8 | 2 | 1 | 2 | 1 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0005g0135 | a0001 | c0001 | t0005 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0005g0136 | a0001 | c0001 | t0005 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0007g0026 | a0001 | c0001 | t0007 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0008g0127 | a0001 | c0001 | t0008 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0001t0009g0123 | a0001 | c0001 | t0009 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0002t0003g0013 | a0001 | c0002 | t0003 | g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0002t0003g0090 | a0001 | c0002 | t0003 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0003t0006g0022 | a0001 | c0003 | t0006 | g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0004t0004g0130 | a0001 | c0004 | t0004 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0001c0004t0004g0131 | a0001 | c0004 | t0004 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
a0002c0005t0001g0001 | a0002 | c0005 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCE1_chr4_145093311_145134524 | ABCE1 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01243 | hp1 | a0001 | c0003 | t0006 | g0022 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02723 | hp1 | a0001 | c0003 | t0006 | g0022 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02818 | hp1 | a0001 | c0004 | t0004 | g0130 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18982 | hp1 | a0002 | c0005 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19043 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19070 | hp2 | a0001 | c0001 | t0008 | g0127 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0123 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | ABCE1_chr4_145093311_145134524 | ABCE1 |
HG06807 | hp2 | a0001 | c0004 | t0004 | g0131 | AFR | USA | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | ABCE1_chr4_145093311_145134524 | ABCE1 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0028 | REF | REF | ABCE1_chr4_145093311_145134524 | ABCE1 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0083 | REF | REF | ABCE1_chr4_145093311_145134524 | ABCE1 |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145123031
|
G | A | 1 | a0002 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1274G>A | p.Arg425His | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 14/18 | 1410/3887 | 1274/1800 | 425/599 | chr4 | 145123031 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145109174
|
A | T | 1 | a0001c0004 | 2 | HG02818.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.330A>T | p.Gly110Gly | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/18 | 466/3887 | 330/1800 | 110/599 | chr4 | 145109174 | ||
chr4:145112254
|
G | A | 1 | a0001c0002 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.726G>A | p.Glu242Glu | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/18 | 862/3887 | 726/1800 | 242/599 | chr4 | 145112254 | ||
chr4:145123265
|
C | T | 2 | a0001c0003a0001c0004 | 4 | HG01243.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1425C>T | p.Cys475Cys | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 15/18 | 1561/3887 | 1425/1800 | 475/599 | chr4 | 145123265 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145127583
|
G | C | 1 | a0001c0001t0007 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 10 | chr4 | 145127583 | |||||
chr4:145127688
|
A | G | 1 | a0001c0003t0006 | 2 | HG01243.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 115 | chr4 | 145127688 | |||||
chr4:145127757
|
C | T | 1 | a0001c0001t0005 | 2 | HG01884.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 184 | chr4 | 145127757 | |||||
chr4:145128169
|
G | A | 1 | a0001c0004t0004 | 2 | HG02818.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*596G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 596 | chr4 | 145128169 | |||||
chr4:145128631
|
C | G | 1 | a0001c0002t0003 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1058C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1058 | chr4 | 145128631 | |||||
chr4:145128770
|
G | A | 1 | a0001c0004t0004 | 2 | HG02818.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1197 | chr4 | 145128770 | |||||
chr4:145129022
|
T | A | 1 | a0001c0001t0008 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1449T>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1449 | chr4 | 145129022 | |||||
chr4:145129307
|
G | A | 1 | a0001c0001t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1734 | chr4 | 145129307 | |||||
chr4:145129350
|
T | C | 1 | a0001c0001t0002 | 4 | HG01243.hp2 HG02615.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1777T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 18/18 | 1777 | chr4 | 145129350 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145098543
|
G | T | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+124G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145098543 | ||||||
chr4:145098544
|
C | T | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+125C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145098544 | ||||||
chr4:145098549
|
G | A | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+130G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145098549 | ||||||
chr4:145098735
|
AAACCTGC others(8): Show |
A | 4 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 8 | HG01261.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+319_-28+333del others(15): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145098735 | |||||
chr4:145099019
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-28+600C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145099019 | ||||||
chr4:145099159
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-28+740C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145099159 | ||||||
chr4:145099698
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-28+1279T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145099698 | ||||||
chr4:145100049
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-28+1630T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100049 | ||||||
chr4:145100246
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-28+1827C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100246 | ||||||
chr4:145100298
|
G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-28+1879G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100298 | ||||||
chr4:145100446
|
C | T | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+2027C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100446 | ||||||
chr4:145100538
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-28+2119G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100538 | ||||||
chr4:145100580
|
AAGTTGTC others(14): Show |
A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-28+2164_-28+2184d others(23): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145100580 | |||||
chr4:145100630
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-28+2211A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100630 | ||||||
chr4:145100646
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28+2227A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145100646 | ||||||
chr4:145101061
|
A | T | 1 | a0001c0001t0008g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-28+2642A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101061 | ||||||
chr4:145101073
|
A | AT | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0032others(4): Show | 13 | HG01261.hp1 HG01261.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-28+2654_-28+2655i others(3): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101073 | ||||||
chr4:145101073
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0057 | 5 | HG01358.hp1 HG02257.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+2654A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101073 | ||||||
chr4:145101225
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28+2806T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101225 | ||||||
chr4:145101498
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-27-2888G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101498 | ||||||
chr4:145101669
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-27-2717G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101669 | ||||||
chr4:145101739
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(16): Show | 35 | HG00621.hp2 HG00741.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.-27-2647T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145101739 | ||||||
chr4:145102075
|
T | G | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-2311T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102075 | ||||||
chr4:145102110
|
C | G | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-2276C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102110 | ||||||
chr4:145102213
|
G | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-2173G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102213 | ||||||
chr4:145102493
|
A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01257.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-27-1893A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102493 | ||||||
chr4:145102696
|
A | G | 1 | a0001c0001t0001g0021 | 2 | NA18969.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-27-1690A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102696 | ||||||
chr4:145102748
|
G | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27-1638G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102748 | ||||||
chr4:145102772
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0032others(3): Show | 12 | HG01261.hp2 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27-1614T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102772 | ||||||
chr4:145102808
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-27-1578G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145102808 | ||||||
chr4:145103029
|
CAG | C | 3 | a0001c0001t0001g0125a0001c0004t0004g0130a0001c0004t0004g0131 | 3 | HG02630.hp2 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-1356_-27-1355d others(4): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103029 | ||||||
chr4:145103123
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-27-1263A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103123 | ||||||
chr4:145103208
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-27-1178A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103208 | ||||||
chr4:145103620
|
G | A | 1 | a0001c0001t0008g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-27-766G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103620 | ||||||
chr4:145103628
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-27-758C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103628 | ||||||
chr4:145103766
|
G | GT | 57 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 97 | HG00673.hp1 HG01069.hp2 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.-27-605dupT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145103766 | |||||
chr4:145103766
|
GT | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 8 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-605delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145103766 | |||||
chr4:145103806
|
G | C | 1 | a0001c0001t0001g0098 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-27-580G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145103806 | ||||||
chr4:145104201
|
A | G | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27-185A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145104201 | ||||||
chr4:145104262
|
AT | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0004t0004g0130others(1): Show | 5 | HG02559.hp1 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-114delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 145104262 | |||||
chr4:145104331
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0005g0135others(1): Show | 5 | HG01884.hp1 HG02572.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-55T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 1/17 | chr4 | 145104331 | ||||||
chr4:145105041
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.103+526G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105041 | ||||||
chr4:145105046
|
ATAGAATT others(9): Show |
A | 1 | a0001c0001t0001g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.103+544_104-531del others(16): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr4 | 145105046 | |||||
chr4:145105059
|
C | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.103+544C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105059 | ||||||
chr4:145105309
|
A | T | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.104-296A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105309 | ||||||
chr4:145105496
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.104-109G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 2/17 | chr4 | 145105496 | ||||||
chr4:145105908
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0025 | 5 | HG01192.hp2 HG02055.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+218C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145105908 | ||||||
chr4:145105939
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.189+249C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145105939 | ||||||
chr4:145105955
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189+265A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145105955 | ||||||
chr4:145106153
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0134 | 5 | HG01261.hp2 HG02055.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+463C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106153 | ||||||
chr4:145106225
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189+535G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106225 | ||||||
chr4:145106282
|
G | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0035others(4): Show | 15 | HG00280.hp1 HG01081.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+592G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106282 | ||||||
chr4:145106409
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.189+719G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106409 | ||||||
chr4:145106634
|
G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.189+944G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106634 | ||||||
chr4:145106648
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.189+958T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106648 | ||||||
chr4:145106690
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0100 | 2 | NA18942.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+1000T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145106690 | ||||||
chr4:145107164
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.190-851A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107164 | ||||||
chr4:145107192
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG01074.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.190-823G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107192 | ||||||
chr4:145107290
|
G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.190-725G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107290 | ||||||
chr4:145107326
|
A | G | 1 | a0001c0001t0009g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.190-689A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107326 | ||||||
chr4:145107622
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-393A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107622 | ||||||
chr4:145107636
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.190-379G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107636 | ||||||
chr4:145107671
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18952.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.190-344A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107671 | ||||||
chr4:145107934
|
A | C | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.190-81A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 3/17 | chr4 | 145107934 | ||||||
chr4:145108137
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.287+25C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108137 | ||||||
chr4:145108260
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287+148T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108260 | ||||||
chr4:145108449
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.287+337C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108449 | ||||||
chr4:145108555
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.287+443A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108555 | ||||||
chr4:145108751
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.288-381A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108751 | ||||||
chr4:145108932
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18968.hp2 NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.288-200A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 4/17 | chr4 | 145108932 | ||||||
chr4:145109313
|
G | T | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.405+64G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109313 | ||||||
chr4:145109396
|
T | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0037 | 3 | NA18947.hp2 NA19010.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.405+147T>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109396 | ||||||
chr4:145109459
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405+210T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109459 | ||||||
chr4:145109539
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.405+290A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109539 | ||||||
chr4:145109551
|
T | G | 1 | a0001c0001t0001g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.405+302T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109551 | ||||||
chr4:145109601
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.405+352A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109601 | ||||||
chr4:145109672
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0009g0123 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.405+423T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | chr4 | 145109672 | ||||||
chr4:145110084
|
AT | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0037others(6): Show | 9 | HG00558.hp1 HG00558.hp2 HG02451.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.406-3delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 145110084 | |||||
chr4:145110244
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02559.hp1 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.543+4G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110244 | ||||||
chr4:145110275
|
A | G | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543+35A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110275 | ||||||
chr4:145110299
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0009g0123 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.543+59A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110299 | ||||||
chr4:145110350
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.544-25A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 6/17 | chr4 | 145110350 | ||||||
chr4:145110451
|
G | T | 1 | a0001c0001t0001g0031 | 2 | HG03139.hp1 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.613+7G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 7/17 | chr4 | 145110451 | ||||||
chr4:145110568
|
C | T | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.613+124C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 7/17 | chr4 | 145110568 | ||||||
chr4:145110578
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.613+134C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 7/17 | chr4 | 145110578 | ||||||
chr4:145111086
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.710+22G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111086 | ||||||
chr4:145111123
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.710+59A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111123 | ||||||
chr4:145111424
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0009g0123 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.710+360C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111424 | ||||||
chr4:145111530
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.710+466G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111530 | ||||||
chr4:145111580
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.710+516G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111580 | ||||||
chr4:145111779
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.711-460T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111779 | ||||||
chr4:145111790
|
C | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.711-449C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111790 | ||||||
chr4:145111803
|
T | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.711-436T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145111803 | ||||||
chr4:145112216
|
CT | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0030others(22): Show | 32 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.711-6delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 145112216 | |||||
chr4:145112216
|
CTT | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(35): Show | 73 | HG00673.hp1 HG01069.hp2 HG01070.hp1 others(70): Show |
splice_region_variant&intron_variant | LOW | c.711-7_711-6delTT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 145112216 | |||||
chr4:145112221
|
T | C | 1 | a0001c0004t0004g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711-18T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 8/17 | chr4 | 145112221 | ||||||
chr4:145112468
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.800+140T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112468 | ||||||
chr4:145112562
|
T | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0063others(4): Show | 10 | HG01496.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.800+234T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112562 | ||||||
chr4:145112655
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.800+327G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112655 | ||||||
chr4:145112660
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0023others(3): Show | 15 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.800+332C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112660 | ||||||
chr4:145112727
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.800+399G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112727 | ||||||
chr4:145112956
|
T | G | 1 | a0001c0001t0001g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.800+628T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145112956 | ||||||
chr4:145113023
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.800+695T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113023 | ||||||
chr4:145113047
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.800+719A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113047 | ||||||
chr4:145113109
|
G | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.800+781G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113109 | ||||||
chr4:145113111
|
A | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 63 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.800+783A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113111 | ||||||
chr4:145113177
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.800+849G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113177 | ||||||
chr4:145113211
|
G | C | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.800+883G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113211 | ||||||
chr4:145113244
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.800+916C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113244 | ||||||
chr4:145113252
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.800+924A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113252 | ||||||
chr4:145113462
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0023others(3): Show | 15 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.800+1134T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113462 | ||||||
chr4:145113879
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.800+1551C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145113879 | ||||||
chr4:145114215
|
G | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.800+1887G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114215 | ||||||
chr4:145114522
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.800+2194A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114522 | ||||||
chr4:145114615
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.800+2287G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114615 | ||||||
chr4:145114885
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.801-2408A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114885 | ||||||
chr4:145114994
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.801-2299G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145114994 | ||||||
chr4:145115012
|
G | A | 1 | a0001c0001t0005g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.801-2281G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115012 | ||||||
chr4:145115210
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0107 | 2 | HG02148.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.801-2083G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115210 | ||||||
chr4:145115236
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.801-2057G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115236 | ||||||
chr4:145115690
|
T | C | 1 | a0001c0001t0001g0028 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.801-1603T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145115690 | ||||||
chr4:145116168
|
G | A | 1 | a0001c0001t0001g0007 | 5 | HG00099.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1125G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116168 | ||||||
chr4:145116282
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.801-1011T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116282 | ||||||
chr4:145116297
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.801-996C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116297 | ||||||
chr4:145116483
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0053others(1): Show | 4 | HG01934.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-810C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116483 | ||||||
chr4:145116531
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.801-762T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116531 | ||||||
chr4:145116686
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.801-607T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116686 | ||||||
chr4:145116795
|
T | C | 2 | a0001c0002t0003g0013a0001c0002t0003g0090 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-498T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116795 | ||||||
chr4:145116838
|
T | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.801-455T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116838 | ||||||
chr4:145116913
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.801-380C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145116913 | ||||||
chr4:145117252
|
G | C | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.801-41G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 9/17 | chr4 | 145117252 | ||||||
chr4:145117570
|
A | G | 1 | a0001c0001t0009g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.922+156A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145117570 | ||||||
chr4:145117639
|
A | G | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.922+225A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145117639 | ||||||
chr4:145117696
|
CTGCAGTA others(9): Show |
C | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 64 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.922+284_922+299del others(16): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145117696 | |||||
chr4:145118253
|
C | CT | 2 | a0001c0001t0001g0011a0001c0003t0006g0022 | 5 | HG01192.hp2 HG01243.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.922+853dupT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145118253 | |||||
chr4:145118253
|
CT | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0066others(2): Show | 6 | HG01070.hp2 HG01515.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.922+853delT | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145118253 | |||||
chr4:145118582
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.922+1168A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118582 | ||||||
chr4:145118634
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.922+1220T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118634 | ||||||
chr4:145118692
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.923-1240C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118692 | ||||||
chr4:145118729
|
G | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.923-1203G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118729 | ||||||
chr4:145118923
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.923-1009C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145118923 | ||||||
chr4:145119163
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0067 | 3 | HG00741.hp2 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.923-769G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119163 | ||||||
chr4:145119225
|
C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(30): Show | 65 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.923-707C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119225 | ||||||
chr4:145119238
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.923-694T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119238 | ||||||
chr4:145119265
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.923-667A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119265 | ||||||
chr4:145119451
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.923-481A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119451 | ||||||
chr4:145119589
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.923-343A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119589 | ||||||
chr4:145119706
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.923-226A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | chr4 | 145119706 | ||||||
chr4:145119771
|
TTAAA | T | 2 | a0001c0002t0003g0013a0001c0002t0003g0090 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-158_923-155del others(4): Show |
ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 145119771 | |||||
chr4:145120200
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1144+47G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120200 | ||||||
chr4:145120318
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1144+165G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120318 | ||||||
chr4:145120357
|
C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0065others(1): Show | 10 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144+204C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120357 | ||||||
chr4:145120559
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144+406A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120559 | ||||||
chr4:145120648
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1144+495A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120648 | ||||||
chr4:145120989
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1145-185T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 11/17 | chr4 | 145120989 | ||||||
chr4:145121293
|
G | C | 1 | a0001c0001t0001g0007 | 5 | HG00099.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1205-40G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 12/17 | chr4 | 145121293 | ||||||
chr4:145122415
|
C | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1264-606C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 13/17 | chr4 | 145122415 | ||||||
chr4:145122656
|
T | A | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1264-365T>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 13/17 | chr4 | 145122656 | ||||||
chr4:145122774
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1264-247G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 13/17 | chr4 | 145122774 | ||||||
chr4:145123373
|
C | A | 2 | a0001c0004t0004g0130a0001c0004t0004g0131 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1517+16C>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 15/17 | chr4 | 145123373 | ||||||
chr4:145123387
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1517+30A>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 15/17 | chr4 | 145123387 | ||||||
chr4:145123783
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1640+183A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145123783 | ||||||
chr4:145123828
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1640+228C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145123828 | ||||||
chr4:145123841
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1640+241G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145123841 | ||||||
chr4:145124025
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0097 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1640+425A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124025 | ||||||
chr4:145124338
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1641-652T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124338 | ||||||
chr4:145124533
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1641-457G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124533 | ||||||
chr4:145124616
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1641-374T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124616 | ||||||
chr4:145124645
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1641-345C>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124645 | ||||||
chr4:145124986
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
splice_region_variant&intron_variant | LOW | c.1641-4T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 16/17 | chr4 | 145124986 | ||||||
chr4:145125237
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1752+136G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125237 | ||||||
chr4:145125476
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025 | 7 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+375A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125476 | ||||||
chr4:145125857
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0005g0135others(1): Show | 5 | HG01884.hp1 HG02572.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1752+756C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125857 | ||||||
chr4:145125913
|
C | T | 1 | a0001c0003t0006g0022 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1752+812C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125913 | ||||||
chr4:145125935
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1752+834G>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145125935 | ||||||
chr4:145126155
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1752+1054T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126155 | ||||||
chr4:145126247
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1752+1146G>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126247 | ||||||
chr4:145126326
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0126 | 4 | HG02630.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1200A>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126326 | ||||||
chr4:145126363
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1753-1163C>T | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126363 | ||||||
chr4:145126429
|
G | A | 1 | a0001c0002t0003g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1753-1097G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126429 | ||||||
chr4:145126835
|
T | C | 1 | a0001c0001t0009g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1753-691T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126835 | ||||||
chr4:145126971
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(14): Show | 33 | HG00621.hp2 HG01175.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1753-555G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145126971 | ||||||
chr4:145127086
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1753-440A>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127086 | ||||||
chr4:145127402
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(29): Show | 64 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1753-124T>C | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127402 | ||||||
chr4:145127431
|
T | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1753-95T>G | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127431 | ||||||
chr4:145127457
|
G | A | 2 | a0001c0002t0003g0013a0001c0002t0003g0090 | 4 | HG02145.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753-69G>A | ABCE1 | ENSG00000164163.11 | transcript | ENST00000296577.9 | protein_coding | 17/17 | chr4 | 145127457 |