geneid | 3574 |
---|---|
ensemblid | ENSG00000104432.15 |
hgncid | 6023 |
symbol | IL7 |
name | interleukin 7 |
refseq_nuc | NM_000880.4 |
refseq_prot | NP_000871.1 |
ensembl_nuc | ENST00000263851.9 |
ensembl_prot | ENSP00000263851.4 |
mane_status | MANE Select |
chr | chr8 |
start | 78732772 |
end | 78805463 |
strand | - |
ver | v1.2 |
region | chr8:78732772-78805463 |
region5000 | chr8:78727772-78810463 |
regionname0 | IL7_chr8_78732772_78805463 |
regionname5000 | IL7_chr8_78727772_78810463 |
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 | 177 | 261 | 84 | 48 | 94 | 14 | 19 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0002 | 0/0 | 177 | 3 | 0 | 0 | 0 | 0 | 3 | IL7_chr8_78727772_78810463 | IL7 | 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 | 534 | 261 | 84 | 48 | 94 | 14 | 19 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
c0002 | 0/0 | 534 | 3 | 0 | 0 | 0 | 0 | 3 | IL7_chr8_78727772_78810463 | IL7 | 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 | 1483 | 193 | 51 | 38 | 77 | 10 | 15 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0002 | 0/0 | 1482 | 52 | 24 | 9 | 11 | 3 | 5 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0003 | 0/0 | 1483 | 8 | 7 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0004 | 0/0 | 1483 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0005 | 0/0 | 1482 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0006 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0007 | 0/0 | 1483 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0008 | 0/0 | 1483 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0009 | 0/0 | 1483 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0010 | 0/0 | 1483 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
t0011 | 0/0 | 1483 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | 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 | 7 | 0 | 0 | 7 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0004 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL7_chr8_78727772_78810463 | IL7 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
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 | 261 | 84 | 48 | 94 | 14 | 19 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0002c0002 | a0002 | c0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | IL7_chr8_78727772_78810463 | IL7 | 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 | 190 | 51 | 38 | 77 | 10 | 12 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 52 | 24 | 9 | 11 | 3 | 5 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | copy fasta |
a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | IL7_chr8_78727772_78810463 | IL7 | 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 | 7 | 0 | 0 | 7 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0020 | a0001 | c0001 | t0002 | g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0028 | a0001 | c0001 | t0002 | g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0067 | a0001 | c0001 | t0002 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0090 | a0001 | c0001 | t0002 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0128 | a0001 | c0001 | t0002 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0160 | a0001 | c0001 | t0002 | g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0161 | a0001 | c0001 | t0002 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0162 | a0001 | c0001 | t0002 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0170 | a0001 | c0001 | t0002 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0172 | a0001 | c0001 | t0002 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0173 | a0001 | c0001 | t0002 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0174 | a0001 | c0001 | t0002 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0175 | a0001 | c0001 | t0002 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0176 | a0001 | c0001 | t0002 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0177 | a0001 | c0001 | t0002 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0178 | a0001 | c0001 | t0002 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0179 | a0001 | c0001 | t0002 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0180 | a0001 | c0001 | t0002 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0181 | a0001 | c0001 | t0002 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0184 | a0001 | c0001 | t0002 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0186 | a0001 | c0001 | t0002 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0187 | a0001 | c0001 | t0002 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0193 | a0001 | c0001 | t0002 | g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0194 | a0001 | c0001 | t0002 | g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0002g0211 | a0001 | c0001 | t0002 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0003g0009 | a0001 | c0001 | t0003 | g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0003g0110 | a0001 | c0001 | t0003 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0003g0114 | a0001 | c0001 | t0003 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0003g0122 | a0001 | c0001 | t0003 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0003g0125 | a0001 | c0001 | t0003 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0003g0126 | a0001 | c0001 | t0003 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0004g0214 | a0001 | c0001 | t0004 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0004g0215 | a0001 | c0001 | t0004 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0004g0216 | a0001 | c0001 | t0004 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0005g0011 | a0001 | c0001 | t0005 | g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0006g0030 | a0001 | c0001 | t0006 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0007g0202 | a0001 | c0001 | t0007 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0008g0074 | a0001 | c0001 | t0008 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0009g0046 | a0001 | c0001 | t0009 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0010g0073 | a0001 | c0001 | t0010 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
a0001c0001t0011g0213 | a0001 | c0001 | t0011 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 |
a0002c0002t0001g0019 | a0002 | c0002 | t0001 | g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL7_chr8_78727772_78810463 | IL7 |
a0002c0002t0001g0086 | a0002 | c0002 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | IL7_chr8_78727772_78810463 | IL7 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | IL7_chr8_78727772_78810463 | IL7 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0030 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0213 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | IL7_chr8_78727772_78810463 | IL7 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IL7_chr8_78727772_78810463 | IL7 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0074 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0073 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ASW | IL7_chr8_78727772_78810463 | IL7 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ASW | IL7_chr8_78727772_78810463 | IL7 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | IL7_chr8_78727772_78810463 | IL7 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | IL7_chr8_78727772_78810463 | IL7 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | IL7_chr8_78727772_78810463 | IL7 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | IL7_chr8_78727772_78810463 | IL7 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0203 | REF | REF | IL7_chr8_78727772_78810463 | IL7 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0015 | REF | REF | IL7_chr8_78727772_78810463 | IL7 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:78798167
|
C | T | 1 | a0002 | 3 | HG02735.hp1 HG03669.hp1 HG03834.hp1 |
missense_variant | MODERATE | c.52G>A | p.Val18Ile | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/6 | 593/2016 | 52/534 | 18/177 | chr8 | 78798167 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:78732867
|
T | A | 1 | a0001c0001t0010 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*846A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 6/6 | 846 | chr8 | 78732867 | |||||
chr8:78732960
|
CA | C | 3 | a0001c0001t0002a0001c0001t0005a0001c0001t0006 | 55 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*752delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 6/6 | 752 | chr8 | 78732960 | |||||
chr8:78733130
|
A | C | 1 | a0001c0001t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 6/6 | 583 | chr8 | 78733130 | |||||
chr8:78733259
|
A | G | 1 | a0001c0001t0003 | 8 | HG01109.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*454T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 6/6 | 454 | chr8 | 78733259 | |||||
chr8:78733481
|
A | G | 1 | a0001c0001t0008 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*232T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 6/6 | 232 | chr8 | 78733481 | |||||
chr8:78733527
|
A | G | 1 | a0001c0001t0007 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 6/6 | 186 | chr8 | 78733527 | |||||
chr8:78805006
|
C | G | 1 | a0001c0001t0005 | 2 | NA18943.hp1 NA19070.hp1 |
5_prime_UTR_variant | MODIFIER | c.-84G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/6 | 84 | chr8 | 78805006 | |||||
chr8:78805146
|
T | G | 1 | a0001c0001t0006 | 1 | HG01517.hp1 | 5_prime_UTR_variant | MODIFIER | c.-224A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/6 | 224 | chr8 | 78805146 | |||||
chr8:78805394
|
C | A | 1 | a0001c0001t0011 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-472G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/6 | 472 | chr8 | 78805394 | |||||
chr8:78805407
|
T | C | 1 | a0001c0001t0004 | 3 | HG02071.hp1 NA18947.hp1 NA18959.hp1 |
5_prime_UTR_variant | MODIFIER | c.-485A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/6 | 485 | chr8 | 78805407 | |||||
chr8:78805424
|
A | G | 1 | a0001c0001t0006 | 1 | HG01517.hp1 | 5_prime_UTR_variant | MODIFIER | c.-502T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/6 | 502 | chr8 | 78805424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:78733870
|
T | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02040.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.415-38A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78733870 | ||||||
chr8:78734515
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415-683C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78734515 | ||||||
chr8:78734601
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415-769G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78734601 | ||||||
chr8:78734754
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-922T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78734754 | ||||||
chr8:78734830
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.415-998G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78734830 | ||||||
chr8:78734878
|
G | A | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-1046C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78734878 | ||||||
chr8:78734962
|
A | T | 1 | a0001c0001t0001g0143 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.415-1130T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78734962 | ||||||
chr8:78735160
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0156 | 3 | HG00735.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.414+1314T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735160 | ||||||
chr8:78735260
|
A | AGTT | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.414+1211_414+1213d others(5): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735260 | ||||||
chr8:78735276
|
C | CT | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.414+1197dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735276 | ||||||
chr8:78735276
|
C | CTT | 11 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0001g0092others(8): Show | 11 | HG01255.hp2 HG01943.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+1196_414+1197d others(4): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735276 | ||||||
chr8:78735292
|
T | G | 2 | a0001c0001t0002g0173a0001c0001t0002g0175 | 2 | HG01433.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.414+1182A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735292 | ||||||
chr8:78735292
|
T | TTG | 33 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0027others(30): Show | 38 | HG00323.hp2 HG01069.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.414+1181_414+1182i others(4): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735292 | ||||||
chr8:78735293
|
G | GT | 27 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0029others(24): Show | 34 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.414+1180dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735293 | ||||||
chr8:78735293
|
G | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0027others(35): Show | 44 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.414+1181C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735293 | ||||||
chr8:78735312
|
G | GT | 63 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(60): Show | 74 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.414+1161dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735312 | ||||||
chr8:78735376
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 5 | HG01168.hp1 HG01169.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+1098C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735376 | ||||||
chr8:78735423
|
C | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+1051G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735423 | ||||||
chr8:78735625
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.414+849G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735625 | ||||||
chr8:78735801
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.414+673C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735801 | ||||||
chr8:78735996
|
A | C | 1 | a0001c0001t0002g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.414+478T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78735996 | ||||||
chr8:78736129
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.414+345A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78736129 | ||||||
chr8:78736225
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.414+249A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78736225 | ||||||
chr8:78736230
|
TA | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0101others(20): Show | 28 | HG00738.hp2 HG01069.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.414+243delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78736230 | ||||||
chr8:78736230
|
TAA | T | 58 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(55): Show | 68 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.414+242_414+243del others(2): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78736230 | ||||||
chr8:78736822
|
G | C | 66 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(63): Show | 77 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.361-295C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78736822 | ||||||
chr8:78736886
|
C | G | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-359G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78736886 | ||||||
chr8:78737031
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.361-504C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737031 | ||||||
chr8:78737034
|
G | T | 46 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0020others(43): Show | 55 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.361-507C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737034 | ||||||
chr8:78737181
|
A | G | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-654T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737181 | ||||||
chr8:78737183
|
C | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.361-656G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737183 | ||||||
chr8:78737374
|
A | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.361-847T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737374 | ||||||
chr8:78737466
|
A | G | 3 | a0001c0001t0002g0090a0001c0001t0002g0181a0001c0001t0006g0030 | 3 | HG01517.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.361-939T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737466 | ||||||
chr8:78737484
|
T | C | 2 | a0001c0001t0003g0110a0001c0001t0003g0122 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.361-957A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737484 | ||||||
chr8:78737495
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.361-968T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737495 | ||||||
chr8:78737509
|
A | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-982T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737509 | ||||||
chr8:78737595
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+909G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78737595 | ||||||
chr8:78738405
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.360+99A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78738405 | ||||||
chr8:78738493
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.360+11G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78738493 | ||||||
chr8:78738498
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0083 | 5 | HG00673.hp2 HG02080.hp2 NA18972.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.360+6C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 4/5 | chr8 | 78738498 | ||||||
chr8:78738895
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.229-260C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78738895 | ||||||
chr8:78738906
|
G | A | 43 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0028others(40): Show | 51 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.229-271C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78738906 | ||||||
chr8:78739429
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+573G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739429 | ||||||
chr8:78739500
|
T | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.228+502A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739500 | ||||||
chr8:78739524
|
T | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0108others(5): Show | 10 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.228+478A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739524 | ||||||
chr8:78739547
|
T | C | 8 | a0001c0001t0002g0004a0001c0001t0002g0127a0001c0001t0002g0128others(5): Show | 11 | HG00140.hp2 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.228+455A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739547 | ||||||
chr8:78739591
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.228+411G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739591 | ||||||
chr8:78739681
|
ACT | A | 47 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0020others(44): Show | 56 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.228+319_228+320del others(2): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739681 | ||||||
chr8:78739691
|
C | CA | 6 | a0001c0001t0001g0140a0001c0001t0001g0166a0001c0001t0002g0020others(3): Show | 7 | HG01081.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.228+310dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739691 | ||||||
chr8:78739707
|
G | A | 66 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(63): Show | 77 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.228+295C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739707 | ||||||
chr8:78739729
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.228+273T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739729 | ||||||
chr8:78739847
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.228+155T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739847 | ||||||
chr8:78739899
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.228+103C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739899 | ||||||
chr8:78739959
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.228+43A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 3/5 | chr8 | 78739959 | ||||||
chr8:78740137
|
T | C | 1 | a0001c0001t0001g0021 | 2 | NA18942.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.148-55A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78740137 | ||||||
chr8:78740486
|
G | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(8): Show | 13 | HG01069.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-404C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78740486 | ||||||
chr8:78740553
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.148-471T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78740553 | ||||||
chr8:78741149
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.148-1067A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741149 | ||||||
chr8:78741363
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.148-1281C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741363 | ||||||
chr8:78741456
|
A | G | 1 | a0001c0001t0002g0028 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.148-1374T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741456 | ||||||
chr8:78741471
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.148-1389G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741471 | ||||||
chr8:78741472
|
G | A | 2 | a0001c0001t0002g0136a0001c0001t0002g0211 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.148-1390C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741472 | ||||||
chr8:78741910
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.148-1828T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741910 | ||||||
chr8:78741965
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.148-1883T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78741965 | ||||||
chr8:78742094
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.148-2012C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742094 | ||||||
chr8:78742157
|
C | CA | 10 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0001g0092others(7): Show | 10 | HG00738.hp2 HG01175.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-2076dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742157 | ||||||
chr8:78742157
|
CA | C | 60 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0084others(57): Show | 71 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.148-2076delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742157 | ||||||
chr8:78742418
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-2336C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742418 | ||||||
chr8:78742523
|
A | C | 1 | a0001c0001t0002g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.148-2441T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742523 | ||||||
chr8:78742549
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.148-2467C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742549 | ||||||
chr8:78742568
|
T | C | 22 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0067others(19): Show | 26 | HG00280.hp1 HG00673.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.148-2486A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742568 | ||||||
chr8:78742601
|
A | T | 1 | a0001c0001t0003g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.148-2519T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742601 | ||||||
chr8:78742887
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.148-2805G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742887 | ||||||
chr8:78743157
|
G | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-3075C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743157 | ||||||
chr8:78743187
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.148-3105G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743187 | ||||||
chr8:78743192
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(8): Show | 13 | HG01069.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-3110T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743192 | ||||||
chr8:78743349
|
C | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-3267G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743349 | ||||||
chr8:78743547
|
CTGTT | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-3469_148-3466d others(6): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743547 | ||||||
chr8:78743892
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.148-3810G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743892 | ||||||
chr8:78743931
|
C | G | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-3849G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743931 | ||||||
chr8:78743947
|
C | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(29): Show | 47 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.148-3865G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743947 | ||||||
chr8:78744485
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.148-4403G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78744485 | ||||||
chr8:78744754
|
T | G | 80 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0027others(77): Show | 95 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.148-4672A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78744754 | ||||||
chr8:78744929
|
G | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-4847C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78744929 | ||||||
chr8:78745019
|
A | G | 1 | a0001c0001t0002g0029 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.148-4937T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78745019 | ||||||
chr8:78745028
|
T | C | 74 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0027others(71): Show | 87 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.148-4946A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78745028 | ||||||
chr8:78745263
|
T | G | 8 | a0001c0001t0002g0004a0001c0001t0002g0127a0001c0001t0002g0128others(5): Show | 11 | HG00140.hp2 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-5181A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78745263 | ||||||
chr8:78745274
|
T | C | 44 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0028others(41): Show | 52 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.148-5192A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78745274 | ||||||
chr8:78745431
|
T | C | 66 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(63): Show | 77 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.148-5349A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78745431 | ||||||
chr8:78746051
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(8): Show | 13 | HG01069.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-5969T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746051 | ||||||
chr8:78746224
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0153 | 3 | HG01261.hp1 HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.148-6142C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746224 | ||||||
chr8:78746228
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-6146G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746228 | ||||||
chr8:78746251
|
C | T | 6 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0130others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-6169G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746251 | ||||||
chr8:78746341
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-6259T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746341 | ||||||
chr8:78746554
|
G | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0050a0001c0001t0001g0058others(2): Show | 5 | HG00280.hp2 NA18947.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-6472C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746554 | ||||||
chr8:78746584
|
G | C | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-6502C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746584 | ||||||
chr8:78746671
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(57): Show | 82 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.148-6589A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746671 | ||||||
chr8:78746716
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(8): Show | 13 | HG01069.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-6634T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746716 | ||||||
chr8:78746947
|
T | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(43): Show | 64 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.148-6865A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78746947 | ||||||
chr8:78747162
|
G | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.148-7080C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747162 | ||||||
chr8:78747188
|
C | CT | 60 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0031others(57): Show | 72 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.148-7107dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747188 | ||||||
chr8:78747188
|
C | CTTT | 11 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(8): Show | 13 | HG01069.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-7109_148-7107d others(5): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747188 | ||||||
chr8:78747188
|
CT | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0064a0001c0001t0001g0071others(6): Show | 9 | HG01167.hp1 HG01192.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-7107delA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747188 | ||||||
chr8:78747241
|
A | G | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-7159T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747241 | ||||||
chr8:78747246
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.148-7164G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747246 | ||||||
chr8:78747566
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 104 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.148-7484A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747566 | ||||||
chr8:78747650
|
T | C | 2 | a0001c0001t0003g0110a0001c0001t0003g0122 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.148-7568A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747650 | ||||||
chr8:78748098
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.148-8016C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78748098 | ||||||
chr8:78748255
|
G | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | NA18945.hp1 NA18960.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.148-8173C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78748255 | ||||||
chr8:78748284
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-8202T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78748284 | ||||||
chr8:78748310
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0163others(8): Show | 13 | HG01069.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-8228C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78748310 | ||||||
chr8:78748519
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-8437A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78748519 | ||||||
chr8:78748835
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.148-8753T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78748835 | ||||||
chr8:78749096
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.148-9014T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78749096 | ||||||
chr8:78749372
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 11 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.148-9290G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78749372 | ||||||
chr8:78749469
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.148-9387A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78749469 | ||||||
chr8:78749515
|
A | G | 5 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0130others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-9433T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78749515 | ||||||
chr8:78749571
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0200 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.148-9489C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78749571 | ||||||
chr8:78750061
|
T | G | 2 | a0001c0001t0004g0214a0001c0001t0004g0215 | 2 | NA18947.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.148-9979A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750061 | ||||||
chr8:78750101
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 105 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.148-10019A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750101 | ||||||
chr8:78750234
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.148-10152T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750234 | ||||||
chr8:78750339
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.148-10257T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750339 | ||||||
chr8:78750404
|
GA | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-10323delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750404 | ||||||
chr8:78750532
|
C | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-10450G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750532 | ||||||
chr8:78750608
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-10526C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750608 | ||||||
chr8:78750640
|
G | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.148-10558C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750640 | ||||||
chr8:78750667
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.148-10585G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750667 | ||||||
chr8:78750811
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.148-10729C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750811 | ||||||
chr8:78750818
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-10736G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78750818 | ||||||
chr8:78751053
|
A | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-10971T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751053 | ||||||
chr8:78751091
|
C | CA | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(51): Show | 77 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.148-11010dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751091 | ||||||
chr8:78751091
|
CA | C | 32 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0183others(29): Show | 37 | HG00280.hp1 HG00673.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.148-11010delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751091 | ||||||
chr8:78751125
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-11043T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751125 | ||||||
chr8:78751157
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.148-11075A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751157 | ||||||
chr8:78751173
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 102 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.148-11091C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751173 | ||||||
chr8:78751565
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.148-11483T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751565 | ||||||
chr8:78751982
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0076 | 3 | HG01168.hp1 HG01169.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.148-11900T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78751982 | ||||||
chr8:78752147
|
T | C | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-12065A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752147 | ||||||
chr8:78752248
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 105 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.148-12166C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752248 | ||||||
chr8:78752373
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.148-12291G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752373 | ||||||
chr8:78752414
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0113 | 3 | HG01943.hp1 HG02717.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.148-12332G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752414 | ||||||
chr8:78752642
|
C | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0127a0001c0001t0002g0128others(5): Show | 11 | HG00140.hp2 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-12560G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752642 | ||||||
chr8:78752694
|
G | A | 1 | a0001c0001t0002g0029 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.148-12612C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752694 | ||||||
chr8:78752716
|
G | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-12634C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752716 | ||||||
chr8:78752836
|
C | T | 2 | a0001c0001t0003g0125a0001c0001t0003g0126 | 2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.148-12754G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752836 | ||||||
chr8:78752904
|
T | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-12822A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752904 | ||||||
chr8:78752929
|
ATTTT | A | 5 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0137others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-12851_148-1284 others(8): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752929 | ||||||
chr8:78752991
|
A | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-12909T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78752991 | ||||||
chr8:78753001
|
G | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-12919C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753001 | ||||||
chr8:78753032
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.148-12950C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753032 | ||||||
chr8:78753067
|
CT | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0146a0001c0001t0001g0150others(2): Show | 5 | HG01192.hp2 HG01981.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-12986delA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753067 | ||||||
chr8:78753072
|
T | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 102 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.148-12990A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753072 | ||||||
chr8:78753094
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 102 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.148-13012G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753094 | ||||||
chr8:78753141
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.148-13059G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753141 | ||||||
chr8:78753216
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-13134G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753216 | ||||||
chr8:78753331
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.148-13249G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753331 | ||||||
chr8:78753368
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-13286C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753368 | ||||||
chr8:78753587
|
C | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(24): Show | 33 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.148-13505G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753587 | ||||||
chr8:78753589
|
A | G | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-13507T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753589 | ||||||
chr8:78753709
|
C | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-13627G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753709 | ||||||
chr8:78753799
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 102 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.148-13717G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753799 | ||||||
chr8:78753961
|
G | T | 1 | a0001c0001t0002g0115 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.148-13879C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78753961 | ||||||
chr8:78754389
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 8 | HG01099.hp1 HG01109.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-14307C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78754389 | ||||||
chr8:78754497
|
A | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 119 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.148-14415T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78754497 | ||||||
chr8:78754571
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.148-14489G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78754571 | ||||||
chr8:78754651
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-14569A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78754651 | ||||||
chr8:78754734
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0072 | 3 | HG01433.hp1 HG02258.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.148-14652T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78754734 | ||||||
chr8:78754849
|
T | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-14767A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78754849 | ||||||
chr8:78755010
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.148-14928T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78755010 | ||||||
chr8:78755253
|
T | C | 1 | a0001c0001t0006g0030 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.148-15171A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78755253 | ||||||
chr8:78755648
|
T | TA | 1 | a0001c0001t0001g0003 | 4 | HG02922.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-15567dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78755648 | ||||||
chr8:78755820
|
T | C | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.148-15738A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78755820 | ||||||
chr8:78756209
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0003g0110a0001c0001t0003g0122 | 4 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-16127T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78756209 | ||||||
chr8:78756442
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG00621.hp2 HG02155.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-16360C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78756442 | ||||||
chr8:78756617
|
A | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | HG02055.hp1 HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.148-16535T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78756617 | ||||||
chr8:78756984
|
T | G | 1 | a0001c0001t0001g0007 | 3 | NA18942.hp2 NA18972.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.148-16902A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78756984 | ||||||
chr8:78757026
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.148-16944G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78757026 | ||||||
chr8:78757180
|
G | C | 1 | a0001c0001t0003g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.148-17098C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78757180 | ||||||
chr8:78757206
|
C | T | 6 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0003g0009others(3): Show | 8 | HG01081.hp2 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-17124G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78757206 | ||||||
chr8:78757327
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-17245C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78757327 | ||||||
chr8:78757633
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.148-17551T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78757633 | ||||||
chr8:78757951
|
T | G | 1 | a0001c0001t0002g0119 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.148-17869A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78757951 | ||||||
chr8:78758152
|
C | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 119 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.148-18070G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758152 | ||||||
chr8:78758155
|
T | A | 2 | a0001c0001t0002g0117a0001c0001t0002g0120 | 2 | HG01884.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.148-18073A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758155 | ||||||
chr8:78758260
|
A | G | 2 | a0001c0001t0003g0110a0001c0001t0003g0122 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.148-18178T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758260 | ||||||
chr8:78758281
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0156a0001c0001t0001g0157 | 4 | HG00323.hp2 HG00735.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-18199C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758281 | ||||||
chr8:78758309
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-18227C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758309 | ||||||
chr8:78758324
|
T | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-18242A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758324 | ||||||
chr8:78758441
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.148-18359G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758441 | ||||||
chr8:78758486
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.148-18404G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758486 | ||||||
chr8:78758681
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-18599G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758681 | ||||||
chr8:78758832
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 105 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.148-18750G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758832 | ||||||
chr8:78759057
|
T | TC | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(62): Show | 87 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.148-18976dupG | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759057 | ||||||
chr8:78759193
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-19111T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759193 | ||||||
chr8:78759216
|
C | CT | 7 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0108others(4): Show | 9 | HG01109.hp2 HG02040.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-19135dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759216 | ||||||
chr8:78759216
|
C | CTT | 30 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0027others(27): Show | 37 | HG00738.hp2 HG01069.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.148-19136_148-1913 others(6): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759216 | ||||||
chr8:78759216
|
C | CTTT | 40 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(37): Show | 52 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.148-19137_148-1913 others(7): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759216 | ||||||
chr8:78759216
|
C | CTTTT | 7 | a0001c0001t0001g0001a0001c0001t0001g0142a0001c0001t0001g0143others(4): Show | 13 | HG00621.hp1 HG02056.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-19138_148-1913 others(8): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759216 | ||||||
chr8:78759248
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 106 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.148-19166T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759248 | ||||||
chr8:78759401
|
T | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-19319A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759401 | ||||||
chr8:78759417
|
GA | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 111 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.148-19336delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759417 | ||||||
chr8:78759475
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-19393G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759475 | ||||||
chr8:78759560
|
T | A | 2 | a0001c0001t0003g0125a0001c0001t0003g0126 | 2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.148-19478A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759560 | ||||||
chr8:78759715
|
T | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 12 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.148-19633A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759715 | ||||||
chr8:78759902
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.148-19820C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759902 | ||||||
chr8:78759926
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-19844T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759926 | ||||||
chr8:78760047
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.148-19965A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760047 | ||||||
chr8:78760132
|
TAA | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 59 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.148-20052_148-2005 others(6): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760132 | ||||||
chr8:78760147
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 106 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.148-20065A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760147 | ||||||
chr8:78760163
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.148-20081C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760163 | ||||||
chr8:78760194
|
G | C | 2 | a0001c0001t0003g0110a0001c0001t0003g0122 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.148-20112C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760194 | ||||||
chr8:78760212
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-20130C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760212 | ||||||
chr8:78760319
|
ACGCTTTC others(3): Show |
A | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.148-20247_148-2023 others(14): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760319 | ||||||
chr8:78760322
|
C | T | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.148-20240G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760322 | ||||||
chr8:78760327
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.148-20245T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760327 | ||||||
chr8:78760341
|
C | T | 5 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | HG00738.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-20259G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760341 | ||||||
chr8:78760417
|
G | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 59 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.148-20335C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760417 | ||||||
chr8:78760418
|
T | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 59 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.148-20336A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760418 | ||||||
chr8:78760517
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.148-20435C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760517 | ||||||
chr8:78760570
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.148-20488T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760570 | ||||||
chr8:78760643
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.148-20561C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760643 | ||||||
chr8:78760706
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.148-20624A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760706 | ||||||
chr8:78760718
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.148-20636T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760718 | ||||||
chr8:78761005
|
T | A | 1 | a0002c0002t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.148-20923A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761005 | ||||||
chr8:78761014
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-20932C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761014 | ||||||
chr8:78761069
|
C | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0137others(2): Show | 5 | HG02965.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-20987G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761069 | ||||||
chr8:78761104
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0086 | 3 | HG02735.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.148-21022G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761104 | ||||||
chr8:78761225
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 8 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-21143T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761225 | ||||||
chr8:78761258
|
A | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-21176T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761258 | ||||||
chr8:78761351
|
CAG | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 7 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-21271_148-2127 others(6): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761351 | ||||||
chr8:78761414
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.148-21332C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761414 | ||||||
chr8:78761562
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(28): Show | 46 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.148-21480C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761562 | ||||||
chr8:78761570
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.148-21488C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761570 | ||||||
chr8:78761612
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 108 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.148-21530G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761612 | ||||||
chr8:78761631
|
C | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-21549G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761631 | ||||||
chr8:78761713
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0086 | 3 | HG02735.hp1 HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.148-21631G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761713 | ||||||
chr8:78761717
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(58): Show | 83 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.148-21635A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761717 | ||||||
chr8:78761772
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148-21690C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761772 | ||||||
chr8:78761772
|
G | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0168a0001c0001t0001g0169 | 4 | HG01069.hp2 HG02145.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-21690C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761772 | ||||||
chr8:78761903
|
A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 8 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-21821T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78761903 | ||||||
chr8:78762496
|
C | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-22414G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762496 | ||||||
chr8:78762532
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 59 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.148-22450C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762532 | ||||||
chr8:78762552
|
CG | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 107 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.148-22471delC | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762552 | ||||||
chr8:78762557
|
G | T | 1 | a0001c0001t0002g0029 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.148-22475C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762557 | ||||||
chr8:78762652
|
A | AT | 32 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0031others(29): Show | 38 | HG00673.hp1 HG00673.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.148-22571dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762652 | ||||||
chr8:78762652
|
AT | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.148-22571delA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762652 | ||||||
chr8:78762768
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.148-22686A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762768 | ||||||
chr8:78762947
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01943.hp1 HG02717.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-22865T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762947 | ||||||
chr8:78763027
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.148-22945C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763027 | ||||||
chr8:78763149
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148-23067C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763149 | ||||||
chr8:78763228
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-23146G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763228 | ||||||
chr8:78763349
|
G | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-23267C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763349 | ||||||
chr8:78763355
|
A | C | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-23273T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763355 | ||||||
chr8:78763408
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-23326G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763408 | ||||||
chr8:78763763
|
A | G | 1 | a0001c0001t0001g0013 | 2 | HG00673.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.148-23681T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763763 | ||||||
chr8:78763766
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-23684G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763766 | ||||||
chr8:78764211
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148-24129A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764211 | ||||||
chr8:78764256
|
T | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-24174A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764256 | ||||||
chr8:78764299
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.148-24217A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764299 | ||||||
chr8:78764630
|
C | T | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.148-24548G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764630 | ||||||
chr8:78764635
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.148-24553T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764635 | ||||||
chr8:78764642
|
T | C | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-24560A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764642 | ||||||
chr8:78764716
|
G | A | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-24634C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764716 | ||||||
chr8:78764720
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.148-24638T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764720 | ||||||
chr8:78764898
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 8 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-24816C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78764898 | ||||||
chr8:78765076
|
G | C | 3 | a0001c0001t0002g0175a0001c0001t0002g0186a0001c0001t0002g0187 | 3 | HG00673.hp1 HG02015.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.148-24994C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78765076 | ||||||
chr8:78765357
|
T | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(29): Show | 47 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.148-25275A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78765357 | ||||||
chr8:78765490
|
C | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-25408G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78765490 | ||||||
chr8:78765571
|
T | C | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-25489A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78765571 | ||||||
chr8:78765733
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-25651C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78765733 | ||||||
chr8:78765801
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.148-25719G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78765801 | ||||||
chr8:78766151
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-26069C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766151 | ||||||
chr8:78766280
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-26198T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766280 | ||||||
chr8:78766292
|
A | C | 1 | a0001c0001t0002g0090 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.148-26210T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766292 | ||||||
chr8:78766758
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01943.hp1 HG02717.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-26676T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766758 | ||||||
chr8:78766838
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.148-26756T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766838 | ||||||
chr8:78766926
|
T | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-26844A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766926 | ||||||
chr8:78767003
|
C | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-26921G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767003 | ||||||
chr8:78767098
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.148-27016G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767098 | ||||||
chr8:78767250
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.148-27168A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767250 | ||||||
chr8:78767331
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.148-27249T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767331 | ||||||
chr8:78767405
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.148-27323C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767405 | ||||||
chr8:78767545
|
T | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-27463A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767545 | ||||||
chr8:78767566
|
CTT | C | 3 | a0001c0001t0002g0020a0001c0001t0003g0110a0001c0001t0003g0122 | 4 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-27486_148-2748 others(6): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767566 | ||||||
chr8:78767594
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148-27512G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767594 | ||||||
chr8:78767645
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-27563A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767645 | ||||||
chr8:78767782
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.148-27700A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767782 | ||||||
chr8:78767973
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.148-27891G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767973 | ||||||
chr8:78767974
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 98 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.148-27892A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78767974 | ||||||
chr8:78768000
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148-27918A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768000 | ||||||
chr8:78768020
|
G | A | 8 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-27938C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768020 | ||||||
chr8:78768078
|
C | T | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-27996G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768078 | ||||||
chr8:78768079
|
GTCCCTAC others(6): Show |
G | 1 | a0001c0001t0002g0179 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.148-28010_148-2799 others(17): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768079 | ||||||
chr8:78768156
|
A | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(60): Show | 86 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.148-28074T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768156 | ||||||
chr8:78768207
|
T | C | 1 | a0001c0001t0001g0012 | 2 | NA18972.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.148-28125A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768207 | ||||||
chr8:78768384
|
C | G | 1 | a0001c0001t0002g0020 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148-28302G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768384 | ||||||
chr8:78768391
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.148-28309A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768391 | ||||||
chr8:78768469
|
G | C | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-28387C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768469 | ||||||
chr8:78768535
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.148-28453A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768535 | ||||||
chr8:78768633
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.148-28551C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768633 | ||||||
chr8:78768696
|
G | A | 1 | a0001c0001t0001g0007 | 3 | NA18942.hp2 NA18972.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.148-28614C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768696 | ||||||
chr8:78768802
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-28720G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768802 | ||||||
chr8:78768925
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.148-28843C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78768925 | ||||||
chr8:78769252
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01943.hp1 HG02717.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+28820A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78769252 | ||||||
chr8:78769418
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+28654A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78769418 | ||||||
chr8:78769481
|
C | T | 4 | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0004g0216others(1): Show | 4 | HG01891.hp2 HG02071.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+28591G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78769481 | ||||||
chr8:78769490
|
C | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+28582G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78769490 | ||||||
chr8:78769700
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147+28372C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78769700 | ||||||
chr8:78769846
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.147+28226T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78769846 | ||||||
chr8:78770344
|
C | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+27728G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770344 | ||||||
chr8:78770364
|
TA | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 124 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.147+27707delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770364 | ||||||
chr8:78770378
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 124 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.147+27694G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770378 | ||||||
chr8:78770624
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.147+27448C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770624 | ||||||
chr8:78770714
|
C | T | 7 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(4): Show | 7 | HG02071.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+27358G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770714 | ||||||
chr8:78770733
|
T | C | 22 | a0001c0001t0001g0082a0001c0001t0001g0185a0001c0001t0001g0210others(19): Show | 25 | HG00280.hp1 HG00673.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.147+27339A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770733 | ||||||
chr8:78770750
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.147+27322C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770750 | ||||||
chr8:78770751
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.147+27321T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770751 | ||||||
chr8:78770770
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+27302G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770770 | ||||||
chr8:78770869
|
C | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+27203G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770869 | ||||||
chr8:78771017
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+27055C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771017 | ||||||
chr8:78771161
|
AAAACCTC others(82): Show |
A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+26822_147+2691 others(93): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771161 | ||||||
chr8:78771204
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.147+26868G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771204 | ||||||
chr8:78771252
|
A | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+26820T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771252 | ||||||
chr8:78771330
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.147+26742T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771330 | ||||||
chr8:78771395
|
C | T | 6 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0003g0009others(3): Show | 8 | HG01081.hp2 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+26677G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771395 | ||||||
chr8:78771491
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | NA18945.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.147+26581C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771491 | ||||||
chr8:78771505
|
C | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+26567G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771505 | ||||||
chr8:78771713
|
A | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(64): Show | 90 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.147+26359T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771713 | ||||||
chr8:78771920
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.147+26152A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78771920 | ||||||
chr8:78772141
|
G | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+25931C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78772141 | ||||||
chr8:78772535
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+25537A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78772535 | ||||||
chr8:78772646
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA18947.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.147+25426T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78772646 | ||||||
chr8:78772679
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+25393T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78772679 | ||||||
chr8:78772959
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+25113G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78772959 | ||||||
chr8:78773207
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+24865G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773207 | ||||||
chr8:78773305
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 123 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.147+24767G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773305 | ||||||
chr8:78773553
|
G | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.147+24519C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773553 | ||||||
chr8:78773680
|
T | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+24392A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773680 | ||||||
chr8:78773808
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.147+24264T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773808 | ||||||
chr8:78773980
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0007g0202 | 2 | HG01891.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+24092G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773980 | ||||||
chr8:78774001
|
C | T | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+24071G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78774001 | ||||||
chr8:78774084
|
G | GA | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.147+23987dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78774084 | ||||||
chr8:78774126
|
A | G | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+23946T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78774126 | ||||||
chr8:78774579
|
G | A | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+23493C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78774579 | ||||||
chr8:78775140
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.147+22932T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775140 | ||||||
chr8:78775494
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+22578G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775494 | ||||||
chr8:78775549
|
T | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+22523A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775549 | ||||||
chr8:78775554
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0135others(5): Show | 9 | HG01069.hp2 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+22518C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775554 | ||||||
chr8:78775568
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.147+22504A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775568 | ||||||
chr8:78775590
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.147+22482G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775590 | ||||||
chr8:78775791
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 98 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.147+22281C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775791 | ||||||
chr8:78775862
|
T | G | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+22210A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775862 | ||||||
chr8:78775960
|
G | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+22112C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775960 | ||||||
chr8:78775981
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.147+22091G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775981 | ||||||
chr8:78776088
|
T | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+21984A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776088 | ||||||
chr8:78776154
|
T | A | 1 | a0001c0001t0010g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.147+21918A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776154 | ||||||
chr8:78776250
|
T | C | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+21822A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776250 | ||||||
chr8:78776386
|
C | T | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+21686G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776386 | ||||||
chr8:78776462
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.147+21610C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776462 | ||||||
chr8:78776731
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+21341A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776731 | ||||||
chr8:78776803
|
CA | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+21268delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776803 | ||||||
chr8:78777012
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+21060T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777012 | ||||||
chr8:78777064
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.147+21008G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777064 | ||||||
chr8:78777079
|
TATTATC | T | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+20987_147+2099 others(10): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777079 | ||||||
chr8:78777222
|
C | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+20850G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777222 | ||||||
chr8:78777272
|
G | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+20800C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777272 | ||||||
chr8:78777400
|
C | T | 10 | a0001c0001t0001g0082a0001c0001t0002g0174a0001c0001t0002g0178others(7): Show | 10 | HG00280.hp1 HG01099.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+20672G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777400 | ||||||
chr8:78777431
|
T | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+20641A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777431 | ||||||
chr8:78777502
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.147+20570G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777502 | ||||||
chr8:78777520
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 68 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.147+20552G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777520 | ||||||
chr8:78777578
|
A | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+20494T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777578 | ||||||
chr8:78777587
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.147+20485A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777587 | ||||||
chr8:78777854
|
A | C | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+20218T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777854 | ||||||
chr8:78777921
|
G | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+20151C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777921 | ||||||
chr8:78778099
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.147+19973C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78778099 | ||||||
chr8:78778101
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.147+19971T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78778101 | ||||||
chr8:78778193
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147+19879A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78778193 | ||||||
chr8:78778478
|
G | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+19594C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78778478 | ||||||
chr8:78778570
|
G | T | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.147+19502C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78778570 | ||||||
chr8:78779112
|
G | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+18960C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779112 | ||||||
chr8:78779160
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+18912A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779160 | ||||||
chr8:78779168
|
A | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00558.hp2 HG00597.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+18904T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779168 | ||||||
chr8:78779251
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0128 | 5 | HG00140.hp2 HG01106.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+18821A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779251 | ||||||
chr8:78779405
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+18667A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779405 | ||||||
chr8:78779432
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+18640T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779432 | ||||||
chr8:78779605
|
T | A | 1 | a0001c0001t0008g0074 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.147+18467A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779605 | ||||||
chr8:78779615
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.147+18457C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779615 | ||||||
chr8:78779627
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.147+18445C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779627 | ||||||
chr8:78779650
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.147+18422G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779650 | ||||||
chr8:78779669
|
G | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+18403C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779669 | ||||||
chr8:78779740
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0007g0202 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.147+18332A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779740 | ||||||
chr8:78779806
|
A | G | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+18266T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779806 | ||||||
chr8:78779828
|
G | T | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+18244C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779828 | ||||||
chr8:78779867
|
C | T | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02258.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.147+18205G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78779867 | ||||||
chr8:78780351
|
T | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.147+17721A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780351 | ||||||
chr8:78780385
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+17687C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780385 | ||||||
chr8:78780450
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0114a0001c0001t0003g0125others(1): Show | 6 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+17622G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780450 | ||||||
chr8:78780508
|
C | T | 14 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.147+17564G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780508 | ||||||
chr8:78780645
|
A | T | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+17427T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780645 | ||||||
chr8:78780669
|
A | C | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+17403T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780669 | ||||||
chr8:78780733
|
G | T | 3 | a0001c0001t0001g0100a0001c0001t0002g0172a0001c0001t0002g0173 | 3 | HG01071.hp2 HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.147+17339C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780733 | ||||||
chr8:78780824
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.147+17248T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780824 | ||||||
chr8:78780938
|
A | C | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+17134T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780938 | ||||||
chr8:78780950
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.147+17122G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78780950 | ||||||
chr8:78781260
|
T | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+16812A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78781260 | ||||||
chr8:78781529
|
G | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+16543C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78781529 | ||||||
chr8:78781549
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+16523T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78781549 | ||||||
chr8:78781597
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.147+16475C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78781597 | ||||||
chr8:78781761
|
C | G | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+16311G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78781761 | ||||||
chr8:78781851
|
A | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+16221T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78781851 | ||||||
chr8:78782025
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147+16047A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782025 | ||||||
chr8:78782037
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+16035A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782037 | ||||||
chr8:78782208
|
C | A | 2 | a0001c0001t0001g0101a0001c0001t0007g0202 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.147+15864G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782208 | ||||||
chr8:78782229
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 59 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.147+15843G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782229 | ||||||
chr8:78782308
|
C | CA | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+15763dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782308 | ||||||
chr8:78782402
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 10 | HG01167.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+15670G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782402 | ||||||
chr8:78782653
|
G | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+15419C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782653 | ||||||
chr8:78782818
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.147+15254G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782818 | ||||||
chr8:78782860
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0003g0110a0001c0001t0003g0122 | 4 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+15212G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78782860 | ||||||
chr8:78783031
|
GGCACCA | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(64): Show | 90 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.147+15035_147+1504 others(10): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783031 | ||||||
chr8:78783123
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+14949G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783123 | ||||||
chr8:78783162
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.147+14910A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783162 | ||||||
chr8:78783291
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.147+14781A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783291 | ||||||
chr8:78783292
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.147+14780T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783292 | ||||||
chr8:78783351
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147+14721G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783351 | ||||||
chr8:78783603
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+14469T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783603 | ||||||
chr8:78783751
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.147+14321A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783751 | ||||||
chr8:78783886
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+14186T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78783886 | ||||||
chr8:78784038
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.147+14034G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784038 | ||||||
chr8:78784076
|
C | T | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+13996G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784076 | ||||||
chr8:78784107
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.147+13965T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784107 | ||||||
chr8:78784149
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG00558.hp2 HG00597.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.147+13923G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784149 | ||||||
chr8:78784234
|
C | T | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+13838G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784234 | ||||||
chr8:78784257
|
G | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+13815C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784257 | ||||||
chr8:78784272
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+13800C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784272 | ||||||
chr8:78784440
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+13632G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784440 | ||||||
chr8:78784567
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01943.hp1 HG02717.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+13505T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784567 | ||||||
chr8:78784949
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG00673.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.147+13123G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784949 | ||||||
chr8:78785049
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.147+13023T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78785049 | ||||||
chr8:78785165
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.147+12907T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78785165 | ||||||
chr8:78785248
|
A | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 124 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.147+12824T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78785248 | ||||||
chr8:78785722
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.147+12350C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78785722 | ||||||
chr8:78785902
|
C | T | 1 | a0001c0001t0011g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.147+12170G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78785902 | ||||||
chr8:78786092
|
G | C | 2 | a0001c0001t0003g0110a0001c0001t0003g0122 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.147+11980C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786092 | ||||||
chr8:78786097
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0007g0202 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.147+11975C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786097 | ||||||
chr8:78786171
|
G | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.147+11901C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786171 | ||||||
chr8:78786359
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+11713T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786359 | ||||||
chr8:78786453
|
C | G | 11 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+11619G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786453 | ||||||
chr8:78786777
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+11295G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786777 | ||||||
chr8:78786794
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 126 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.147+11278T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786794 | ||||||
chr8:78786814
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(3): Show | 6 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+11258G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786814 | ||||||
chr8:78786956
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+11116T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786956 | ||||||
chr8:78787015
|
G | T | 1 | a0001c0001t0002g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.147+11057C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787015 | ||||||
chr8:78787186
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.147+10886A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787186 | ||||||
chr8:78787479
|
G | GT | 5 | a0001c0001t0001g0139a0001c0001t0002g0117a0001c0001t0002g0118others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10592dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787479 | ||||||
chr8:78787479
|
G | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02155.hp1 NA18995.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.147+10593C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787479 | ||||||
chr8:78787518
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+10554T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787518 | ||||||
chr8:78787687
|
T | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10385A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787687 | ||||||
chr8:78787696
|
G | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+10376C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787696 | ||||||
chr8:78787697
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.147+10375A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78787697 | ||||||
chr8:78788127
|
G | A | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+9945C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788127 | ||||||
chr8:78788258
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+9814T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788258 | ||||||
chr8:78788415
|
T | C | 1 | a0001c0001t0002g0028 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.147+9657A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788415 | ||||||
chr8:78788580
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.147+9492C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788580 | ||||||
chr8:78788608
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0168a0001c0001t0001g0169 | 4 | HG01069.hp2 HG02145.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+9464A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788608 | ||||||
chr8:78788610
|
T | C | 3 | a0001c0001t0002g0175a0001c0001t0002g0186a0001c0001t0002g0187 | 3 | HG00673.hp1 HG02015.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.147+9462A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788610 | ||||||
chr8:78788636
|
G | A | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+9436C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788636 | ||||||
chr8:78789155
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+8917T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789155 | ||||||
chr8:78789186
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.147+8886A>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789186 | ||||||
chr8:78789448
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(36): Show | 57 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.147+8624G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789448 | ||||||
chr8:78789641
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 90 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.147+8431C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789641 | ||||||
chr8:78789801
|
A | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+8271T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789801 | ||||||
chr8:78789801
|
A | T | 1 | a0001c0001t0002g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.147+8271T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789801 | ||||||
chr8:78789881
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0137others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+8191G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789881 | ||||||
chr8:78789912
|
A | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+8160T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78789912 | ||||||
chr8:78790068
|
C | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0009g0046 | 3 | HG02717.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147+8004G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790068 | ||||||
chr8:78790072
|
TGGAATAG others(15): Show |
T | 3 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0009g0046 | 3 | HG02717.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.147+7978_147+7999d others(24): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790072 | ||||||
chr8:78790097
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.147+7975A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790097 | ||||||
chr8:78790112
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+7960C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790112 | ||||||
chr8:78790214
|
C | T | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.147+7858G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790214 | ||||||
chr8:78790215
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.147+7857C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790215 | ||||||
chr8:78790547
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+7525T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790547 | ||||||
chr8:78790592
|
T | C | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+7480A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790592 | ||||||
chr8:78790614
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147+7458G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790614 | ||||||
chr8:78790642
|
G | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0163others(12): Show | 20 | HG00140.hp2 HG01106.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.147+7430C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790642 | ||||||
chr8:78790645
|
T | G | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.147+7427A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790645 | ||||||
chr8:78790861
|
T | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0156a0001c0001t0001g0157 | 4 | HG00323.hp2 HG00735.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+7211A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790861 | ||||||
chr8:78790875
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.147+7197C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790875 | ||||||
chr8:78790878
|
A | G | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+7194T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790878 | ||||||
chr8:78790921
|
C | CA | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0100others(1): Show | 5 | HG00140.hp1 HG02109.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+7150dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790921 | ||||||
chr8:78790921
|
CA | C | 17 | a0001c0001t0001g0044a0001c0001t0001g0079a0001c0001t0001g0080others(14): Show | 17 | HG00738.hp2 HG01106.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.147+7150delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78790921 | ||||||
chr8:78791043
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.147+7029C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78791043 | ||||||
chr8:78791144
|
A | T | 1 | a0001c0001t0001g0012 | 2 | NA18972.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.147+6928T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78791144 | ||||||
chr8:78791180
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+6892A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78791180 | ||||||
chr8:78791232
|
A | C | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+6840T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78791232 | ||||||
chr8:78792117
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.147+5955C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792117 | ||||||
chr8:78792118
|
G | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+5954C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792118 | ||||||
chr8:78792165
|
G | T | 3 | a0001c0001t0001g0021a0001c0001t0002g0004a0001c0001t0002g0128 | 7 | HG00140.hp2 HG01106.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+5907C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792165 | ||||||
chr8:78792206
|
C | A | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+5866G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792206 | ||||||
chr8:78792271
|
G | A | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+5801C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792271 | ||||||
chr8:78792271
|
G | T | 1 | a0001c0001t0002g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.147+5801C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792271 | ||||||
chr8:78792365
|
C | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.147+5707G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792365 | ||||||
chr8:78792418
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.147+5654T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792418 | ||||||
chr8:78792519
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(28): Show | 46 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.147+5553G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792519 | ||||||
chr8:78792808
|
G | A | 1 | a0001c0001t0002g0029 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.147+5264C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792808 | ||||||
chr8:78792816
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+5256T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792816 | ||||||
chr8:78792899
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 8 | HG01167.hp2 HG01169.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+5173A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792899 | ||||||
chr8:78792940
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.147+5132A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792940 | ||||||
chr8:78792945
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+5127T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78792945 | ||||||
chr8:78793195
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0007g0202 | 2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.147+4877T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78793195 | ||||||
chr8:78793237
|
A | G | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+4835T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78793237 | ||||||
chr8:78793437
|
T | C | 2 | a0001c0001t0003g0009a0001c0001t0003g0114 | 4 | HG01109.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+4635A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78793437 | ||||||
chr8:78793690
|
A | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+4382T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78793690 | ||||||
chr8:78793723
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147+4349G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78793723 | ||||||
chr8:78793777
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+4295A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78793777 | ||||||
chr8:78794031
|
T | G | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+4041A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794031 | ||||||
chr8:78794058
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+4014G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794058 | ||||||
chr8:78794086
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.147+3986T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794086 | ||||||
chr8:78794249
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.147+3823G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794249 | ||||||
chr8:78794305
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+3767T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794305 | ||||||
chr8:78794701
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0191 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.147+3371T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794701 | ||||||
chr8:78794787
|
C | T | 1 | a0001c0001t0002g0028 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.147+3285G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794787 | ||||||
chr8:78794836
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+3236G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794836 | ||||||
chr8:78794905
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0002g0211 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.147+3167G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78794905 | ||||||
chr8:78795176
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.147+2896T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78795176 | ||||||
chr8:78795212
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+2860G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78795212 | ||||||
chr8:78795219
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.147+2853T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78795219 | ||||||
chr8:78795484
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.147+2588A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78795484 | ||||||
chr8:78795948
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.147+2124C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78795948 | ||||||
chr8:78796206
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+1866T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78796206 | ||||||
chr8:78796328
|
A | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0163others(12): Show | 20 | HG00140.hp2 HG01106.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.147+1744T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78796328 | ||||||
chr8:78796707
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.147+1365G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78796707 | ||||||
chr8:78796901
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.147+1171C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78796901 | ||||||
chr8:78796946
|
C | T | 13 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+1126G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78796946 | ||||||
chr8:78796947
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 93 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.147+1125C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78796947 | ||||||
chr8:78797063
|
T | C | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+1009A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797063 | ||||||
chr8:78797096
|
CA | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+975delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797096 | ||||||
chr8:78797256
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+816C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797256 | ||||||
chr8:78797274
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 17 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.147+798C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797274 | ||||||
chr8:78797278
|
G | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02258.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+794C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797278 | ||||||
chr8:78797409
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+663C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797409 | ||||||
chr8:78797479
|
G | C | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.147+593C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797479 | ||||||
chr8:78797675
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.147+397G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797675 | ||||||
chr8:78797691
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(39): Show | 60 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.147+381G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797691 | ||||||
chr8:78797697
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.147+375T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797697 | ||||||
chr8:78797813
|
T | G | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+259A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78797813 | ||||||
chr8:78798345
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0002g0211 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11-137G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798345 | ||||||
chr8:78798347
|
C | T | 1 | a0001c0001t0002g0020 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.11-139G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798347 | ||||||
chr8:78798349
|
A | G | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.11-141T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798349 | ||||||
chr8:78798442
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 17 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.11-234C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798442 | ||||||
chr8:78798477
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0002g0211 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11-269C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798477 | ||||||
chr8:78798644
|
C | CAT | 14 | a0001c0001t0001g0101a0001c0001t0001g0195a0001c0001t0001g0196others(11): Show | 14 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.11-438_11-437dupAT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798644 | ||||||
chr8:78798751
|
G | A | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.11-543C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798751 | ||||||
chr8:78798751
|
G | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.11-543C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798751 | ||||||
chr8:78798976
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.11-768G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78798976 | ||||||
chr8:78799075
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.11-867T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799075 | ||||||
chr8:78799385
|
A | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01943.hp1 HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.11-1177T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799385 | ||||||
chr8:78799573
|
C | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.11-1365G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799573 | ||||||
chr8:78799630
|
C | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG00738.hp2 NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.11-1422G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799630 | ||||||
chr8:78799767
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 7 | HG01099.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.11-1559G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799767 | ||||||
chr8:78799823
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.11-1615C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799823 | ||||||
chr8:78799912
|
T | TA | 7 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.11-1705dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78799912 | ||||||
chr8:78800091
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 131 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.11-1883T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800091 | ||||||
chr8:78800130
|
C | G | 2 | a0001c0001t0002g0028a0001c0001t0007g0202 | 3 | HG01891.hp1 HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.11-1922G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800130 | ||||||
chr8:78800240
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.11-2032G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800240 | ||||||
chr8:78800274
|
G | T | 1 | a0001c0001t0002g0170 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.11-2066C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800274 | ||||||
chr8:78800323
|
G | T | 3 | a0001c0001t0001g0121a0001c0001t0003g0110a0001c0001t0003g0122 | 3 | HG02451.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.11-2115C>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800323 | ||||||
chr8:78800563
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(28): Show | 46 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.11-2355C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800563 | ||||||
chr8:78800698
|
AT | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162 | 3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.11-2491delA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800698 | ||||||
chr8:78800763
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 93 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.11-2555C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800763 | ||||||
chr8:78800871
|
T | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG01106.hp2 HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.11-2663A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800871 | ||||||
chr8:78800882
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 4 | HG01167.hp2 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.11-2674T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78800882 | ||||||
chr8:78801010
|
C | T | 17 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.11-2802G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78801010 | ||||||
chr8:78801112
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.11-2904G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78801112 | ||||||
chr8:78801319
|
A | T | 17 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.11-3111T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78801319 | ||||||
chr8:78801518
|
GAGCCATG others(6): Show |
G | 17 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.11-3323_11-3311del others(13): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78801518 | ||||||
chr8:78801587
|
C | G | 1 | a0001c0001t0006g0030 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.10+3326G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78801587 | ||||||
chr8:78801775
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10+3138C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78801775 | ||||||
chr8:78802318
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 14 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.10+2595G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802318 | ||||||
chr8:78802352
|
A | G | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10+2561T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802352 | ||||||
chr8:78802398
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0002g0160a0001c0001t0002g0161others(1): Show | 4 | HG03688.hp1 HG03831.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+2515C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802398 | ||||||
chr8:78802434
|
C | CT | 18 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 22 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.10+2478dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802434 | ||||||
chr8:78802436
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0002g0192a0001c0001t0002g0193others(1): Show | 4 | HG00280.hp1 HG01255.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+2477A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802436 | ||||||
chr8:78802499
|
C | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0088others(21): Show | 28 | HG00738.hp1 HG01167.hp1 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.10+2414G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802499 | ||||||
chr8:78802515
|
C | G | 7 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(4): Show | 7 | HG00738.hp2 HG02056.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.10+2398G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802515 | ||||||
chr8:78802681
|
C | A | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.10+2232G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802681 | ||||||
chr8:78802764
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.10+2149T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78802764 | ||||||
chr8:78803139
|
G | A | 17 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.10+1774C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78803139 | ||||||
chr8:78803507
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.10+1406C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78803507 | ||||||
chr8:78803510
|
T | G | 1 | a0001c0001t0005g0011 | 2 | NA18943.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.10+1403A>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78803510 | ||||||
chr8:78803734
|
A | C | 1 | a0001c0001t0007g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.10+1179T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78803734 | ||||||
chr8:78804145
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.10+768C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804145 | ||||||
chr8:78804183
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0168a0001c0001t0001g0169 | 4 | HG01069.hp2 HG02145.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+730C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804183 | ||||||
chr8:78804200
|
T | C | 17 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.10+713A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804200 | ||||||
chr8:78804272
|
CAACAAAA others(5): Show |
C | 1 | a0001c0001t0001g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.10+629_10+640delTT others(10): Show |
IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804272 | ||||||
chr8:78804278
|
A | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 148 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.10+635T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804278 | ||||||
chr8:78804301
|
C | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 183 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.10+612G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804301 | ||||||
chr8:78804375
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.10+538G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804375 | ||||||
chr8:78804396
|
A | T | 7 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.10+517T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804396 | ||||||
chr8:78804682
|
T | C | 17 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 17 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.10+231A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804682 | ||||||
chr8:78804712
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.10+201G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804712 | ||||||
chr8:78804738
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.10+175C>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804738 |