Item | Value |
---|---|
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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 177 | 261 | 84 | 48 | 94 | 14 | 19 | 66 | IL7_chr8_78727772_78810463 | IL7 | MFHVS others(172): Show |
chr8 | 78727772 | 78810463 |
a0002 | 0/0 | 177 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | IL7_chr8_78727772_78810463 | IL7 | MFHVS others(172): Show |
chr8 | 78727772 | 78810463 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 531 | 261 | 84 | 48 | 94 | 14 | 19 | IL7_chr8_78727772_78810463 | IL7 | ATGTT others(526): Show |
chr8 | 78727772 | 78810463 | ||
a0002c0002 | 0/0 | 531 | 3 | 0 | 0 | 0 | 0 | 3 | IL7_chr8_78727772_78810463 | IL7 | ATGTT others(526): Show |
chr8 | 78727772 | 78810463 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2016 | 190 | 51 | 38 | 77 | 10 | 12 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0002 | 0/0 | 2015 | 52 | 24 | 9 | 11 | 3 | 5 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2010): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0003 | 0/0 | 2016 | 8 | 7 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0004 | 0/0 | 2016 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0005 | 0/0 | 2015 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2010): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0006 | 0/0 | 2015 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2010): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0007 | 0/0 | 2016 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0008 | 0/0 | 2016 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0009 | 0/0 | 2016 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0010 | 0/0 | 2016 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0001c0001t0011 | 0/0 | 2016 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
a0002c0002t0001 | 0/0 | 2016 | 3 | 0 | 0 | 0 | 0 | 3 | IL7_chr8_78727772_78810463 | IL7 | ACACT others(2011): Show |
chr8 | 78727772 | 78810463 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0004 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0003g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0030 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0213 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0074 | SAS | BEB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0073 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | STU | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ASW | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ASW | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0202 | REF | REF | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0015 | REF | REF | IL7_chr8_78727772_78810463 | IL7 | chr8 | 78727772 | 78810463 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 |
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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:78733870 | T | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0177 |
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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(157): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0124 a0001c0001t0002g0126 |
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 | 32 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0029 others(29): Show |
37 | HG00323.hp2 HG01069.hp2 HG01167.hp2 others(34): 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 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0022 others(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 | 37 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0029 others(34): Show |
43 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(40): 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 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0002g0186 | 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 | a0001c0001t0002g0149 | 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 | a0001c0001t0001g0160 | 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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0101 others(19): Show |
27 | HG00738.hp2 HG01069.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.414+243delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 5/5 | chr8 | 78736230 | |||||||
chr8:78736230 | TAA | T | 58 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | 65 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(62): Show |
76 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(73): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0090 a0001c0001t0002g0132 a0001c0001t0006g0030 |
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 | a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0083 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0021 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0108 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0149 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0191 a0001c0001t0002g0020 others(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 | 65 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(62): Show |
76 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(73): 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 | a0001c0001t0001g0170 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0002g0157 a0001c0001t0002g0211 |
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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
154 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(151): 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 | 9 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0092 others(6): Show |
9 | HG00738.hp2 HG01175.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-2076dupT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78742157 | |||||||
chr8:78742157 | CA | C | 60 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0084 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0148 | 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 | a0001c0001t0002g0183 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0022 a0001c0001t0002g0067 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | a0001c0001t0007g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.148-3267G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78743349 | |||||||
chr8:78743892 | C | T | 1 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0180 |
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 | 79 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0029 others(76): Show |
94 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(91): 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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0002g0022 | 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 | 73 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0029 others(70): Show |
86 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(83): 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 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0149 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0021 others(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 | 65 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(62): Show |
76 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(73): 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 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0174 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0002g0148 a0001c0001t0002g0150 a0001c0001t0002g0151 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0058 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | 59 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0031 others(56): Show |
71 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.148-7107dupA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78747188 | |||||||
chr8:78747188 | C | CTTT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
103 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(100): 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 | a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0139 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0150 a0001c0001t0002g0151 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0200 |
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 | a0001c0001t0004g0214 a0001c0001t0004g0215 |
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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
104 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(101): 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): 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 | a0001c0001t0001g0018 a0001c0001t0001g0076 |
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 | a0001c0001t0007g0203 | 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 | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
104 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(101): 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 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0113 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0149 others(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 | a0001c0001t0002g0022 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0146 a0001c0001t0003g0147 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0180 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
118 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(115): 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 | a0001c0001t0001g0156 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0016 a0001c0001t0001g0072 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0002g0121 | 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 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
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 | a0001c0001t0002g0020 a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0003g0147 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0002g0121 | 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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
118 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(115): 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 | a0001c0001t0002g0119 a0001c0001t0002g0122 |
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 | a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | a0001c0001t0007g0203 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.148-18599G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78758681 | |||||||
chr8:78758832 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
104 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(101): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0029 others(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 | 39 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(36): Show |
51 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(48): 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 | a0001c0001t0001g0001 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0007g0203 | 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 | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
110 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.148-19336delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78759417 | |||||||
chr8:78759475 | C | T | 6 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0146 a0001c0001t0003g0147 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0150 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0002g0184 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.148-20245T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78760327 | |||||||
chr8:78760341 | C | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0002g0151 others(1): Show |
4 | HG00738.hp2 HG01884.hp2 HG03139.hp1 others(1): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0161 | 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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): 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 | a0001c0001t0001g0109 a0001c0001t0001g0112 |
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 | a0001c0001t0003g0143 | 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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(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 | a0002c0002t0001g0019 a0002c0002t0001g0086 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0002c0002t0001g0019 a0002c0002t0001g0086 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0022 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0031 others(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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.148-22571delA | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78762652 | |||||||
chr8:78762768 | T | A | 1 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.148-23146G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78763228 | |||||||
chr8:78763349 | G | A | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0007g0203 | 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 | a0001c0001t0007g0203 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0007g0203 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0126 a0001c0001t0002g0137 a0001c0001t0002g0138 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0156 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.148-26069C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78766151 | |||||||
chr8:78766280 | A | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0007g0203 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0153 | 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 | a0001c0001t0001g0161 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0020 a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0192 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0002g0130 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0002g0130 | 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 | a0001c0001t0007g0203 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | a0001c0001t0004g0214 a0001c0001t0004g0215 a0001c0001t0004g0216 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0131 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+27728G>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770344 | |||||||
chr8:78770364 | TA | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
123 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.147+27707delT | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78770364 | |||||||
chr8:78770378 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
123 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(120): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0136 a0001c0001t0001g0210 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+25393T>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78772679 | |||||||
chr8:78772959 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0007g0203 | 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 | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
122 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(119): 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0144 | 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 | 1 | a0001c0001t0007g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.147+24092G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78773980 | |||||||
chr8:78774001 | C | T | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.147+22932T>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78775140 | |||||||
chr8:78775494 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0155 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0002g0187 | 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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+21341A>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78776731 | |||||||
chr8:78777012 | A | G | 1 | a0001c0001t0001g0188 | 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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0082 a0001c0001t0002g0125 a0001c0001t0002g0129 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+20218T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78777854 | |||||||
chr8:78777921 | G | A | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0001c0001t0002g0150 | 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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0149 |
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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0118 a0001c0001t0001g0180 |
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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0101 a0001c0001t0007g0203 |
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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0114 a0001c0001t0003g0146 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0036 others(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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0100 a0001c0001t0002g0123 a0001c0001t0002g0124 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0174 | 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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0101 a0001c0001t0007g0203 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | |||||||
chr8:78782402 | C | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0002g0020 a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0053 |
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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+13838G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78784234 | |||||||
chr8:78784257 | G | A | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
123 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(120): 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 | a0001c0001t0002g0140 | 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 | a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0101 a0001c0001t0007g0203 |
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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | 10 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+11619G>C | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786453 | |||||||
chr8:78786777 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+11295G>A | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78786777 | |||||||
chr8:78786794 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
125 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(122): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0128 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0160 a0001c0001t0002g0119 a0001c0001t0002g0120 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 |
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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.147+9945C>T | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 2/5 | chr8 | 78788127 | |||||||
chr8:78788258 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | a0001c0001t0002g0126 a0001c0001t0002g0137 a0001c0001t0002g0138 |
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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0009g0046 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0009g0046 |
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 | a0001c0001t0001g0027 | 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 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0188 others(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 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0100 others(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 | 16 | a0001c0001t0001g0044 a0001c0001t0001g0079 a0001c0001t0001g0080 others(13): Show |
16 | HG00738.hp2 HG01106.hp2 HG01255.hp2 others(13): 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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): 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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0023 a0001c0001t0002g0004 a0001c0001t0002g0149 |
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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0002g0148 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(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 | a0001c0001t0002g0022 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0140 | 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 | a0001c0001t0001g0101 a0001c0001t0007g0203 |
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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): 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 | a0001c0001t0003g0009 a0001c0001t0003g0114 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): 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 | a0001c0001t0007g0203 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0180 |
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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0210 a0001c0001t0002g0211 |
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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0188 others(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 | 12 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(9): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0002g0141 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0210 a0001c0001t0002g0211 |
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 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0210 a0001c0001t0002g0211 |
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 | 13 | a0001c0001t0001g0101 a0001c0001t0001g0195 a0001c0001t0001g0196 others(10): Show |
13 | HG00738.hp2 HG01891.hp2 HG02258.hp2 others(10): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 |
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 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
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 | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG00738.hp2 NA20805.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 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
130 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(127): 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 | a0001c0001t0002g0021 a0001c0001t0007g0203 |
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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0142 a0001c0001t0003g0110 a0001c0001t0003g0143 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(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 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0108 |
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 | 16 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(13): 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 | a0001c0001t0001g0193 | 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 | 16 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(13): 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 | 16 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(13): 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0185 a0001c0001t0002g0186 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0087 a0001c0001t0001g0088 others(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 | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG00738.hp2 HG02056.hp1 HG03831.hp1 others(3): 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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | 16 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(13): 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 | a0001c0001t0007g0203 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0193 a0001c0001t0001g0194 |
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 | 16 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(13): 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
147 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.10+635T>G | IL7 | ENSG00000104432.15 | transcript | ENST00000263851.9 | protein_coding | 1/5 | chr8 | 78804278 | |||||||
chr8:78804301 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
182 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(179): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 16 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01891.hp2 HG02056.hp1 others(13): 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 |