Item | Value |
---|---|
geneid | 1385 |
ensemblid | ENSG00000118260.15 |
hgncid | 2345 |
symbol | CREB1 |
name | cAMP responsive element binding protein 1 |
refseq_nuc | NM_004379.5 |
refseq_prot | NP_004370.1 |
ensembl_nuc | ENST00000353267.8 |
ensembl_prot | ENSP00000236995.3 |
mane_status | MANE Select |
chr | chr2 |
start | 207529962 |
end | 207605988 |
strand | + |
ver | v1.2 |
region | chr2:207529962-207605988 |
region5000 | chr2:207524962-207610988 |
regionname0 | CREB1_chr2_207529962_207605988 |
regionname5000 | CREB1_chr2_207524962_207610988 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 981 | 308 | 94 | 60 | 96 | 16 | 40 | CREB1_chr2_207524962_207610988 | CREB1 | ATGAC others(976): Show |
chr2 | 207524962 | 207610988 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10084 | 57 | 1 | 13 | 31 | 3 | 9 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0002 | 0/0 | 10080 | 45 | 7 | 1 | 34 | 0 | 3 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0003 | 0/0 | 10080 | 39 | 3 | 12 | 12 | 2 | 10 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0004 | 0/0 | 10082 | 20 | 5 | 5 | 5 | 1 | 4 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0005 | 0/0 | 10093 | 9 | 2 | 5 | 0 | 0 | 2 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10088): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0006 | 0/0 | 10095 | 9 | 0 | 5 | 0 | 0 | 4 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10090): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0007 | 0/0 | 10080 | 9 | 8 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0008 | 0/0 | 10074 | 8 | 8 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10069): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0009 | 0/0 | 10095 | 6 | 5 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10090): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0010 | 0/0 | 10077 | 6 | 6 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10072): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0011 | 0/0 | 10075 | 6 | 6 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10070): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0012 | 0/0 | 10088 | 5 | 5 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10083): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0013 | 1/0 | 10095 | 4 | 3 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10090): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0014 | 0/0 | 10078 | 4 | 0 | 2 | 0 | 2 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10073): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0015 | 0/0 | 10082 | 4 | 4 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0016 | 0/0 | 10084 | 4 | 0 | 0 | 0 | 0 | 4 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0017 | 0/0 | 10086 | 4 | 0 | 1 | 1 | 0 | 2 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10081): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0018 | 0/0 | 10079 | 4 | 4 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10074): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0019 | 0/0 | 10083 | 4 | 0 | 0 | 4 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10078): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0020 | 0/0 | 10084 | 4 | 0 | 4 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0021 | 0/0 | 10080 | 4 | 0 | 4 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0022 | 0/0 | 10087 | 3 | 3 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10082): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0023 | 0/0 | 10080 | 3 | 3 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0024 | 0/0 | 10077 | 3 | 3 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10072): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0025 | 0/0 | 10082 | 3 | 1 | 2 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0026 | 0/0 | 10082 | 2 | 0 | 0 | 2 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0027 | 0/0 | 10080 | 2 | 0 | 1 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0028 | 0/0 | 10086 | 2 | 0 | 0 | 0 | 2 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10081): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0029 | 0/0 | 10080 | 2 | 0 | 2 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0030 | 0/0 | 10086 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10081): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0031 | 0/0 | 10080 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0032 | 0/0 | 10082 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0033 | 0/0 | 10089 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10084): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0034 | 0/0 | 10093 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10088): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0035 | 0/0 | 10097 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10092): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0036 | 0/1 | 10097 | 1 | 0 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10092): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0037 | 0/0 | 10080 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0038 | 0/0 | 10080 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0039 | 0/0 | 10080 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0040 | 0/0 | 10080 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0041 | 0/0 | 10080 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0042 | 0/0 | 10080 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0043 | 0/0 | 10082 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0044 | 0/0 | 10084 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0045 | 0/0 | 10080 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0046 | 0/0 | 10080 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0047 | 0/0 | 10080 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0048 | 0/0 | 10080 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0049 | 0/0 | 10080 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0050 | 0/0 | 10080 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10075): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0051 | 0/0 | 10077 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10072): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0052 | 0/0 | 10082 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10077): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0053 | 0/0 | 10079 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10074): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0054 | 0/0 | 10084 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0055 | 0/0 | 10084 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0056 | 0/0 | 10084 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10079): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0057 | 0/0 | 10088 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10083): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0058 | 0/0 | 10081 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10076): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0059 | 0/0 | 10086 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10081): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0060 | 0/0 | 10081 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10076): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0061 | 0/0 | 10076 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10071): Show |
chr2 | 207524962 | 207610988 |
a0001c0001t0062 | 0/0 | 10086 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | AGTCG others(10081): Show |
chr2 | 207524962 | 207610988 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0008g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0008g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0009g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0012g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0013g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0013g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0013g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0014g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0014g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0014g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0015g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0015g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0016g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0016g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0017g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0017g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0017g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0018g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0019g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0019g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0020g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0020g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0020g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0021g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0021g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0021g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0021g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0022g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0022g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0022g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0023g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0023g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0023g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0024g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0024g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0024g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0025g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0025g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0026g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0026g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0027g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0027g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0028g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0028g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0029g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0029g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0030g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0031g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0032g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0033g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0034g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0035g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0036g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0037g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0038g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0039g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0040g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0041g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0042g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0043g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0044g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0045g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0046g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0047g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0048g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0049g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0050g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0051g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0052g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0053g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0054g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0055g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0056g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0057g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0058g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0059g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0060g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0061g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
a0001c0001t0062g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0048 | g0166 | EUR | GBR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00099 | hp2 | a0001 | c0001 | t0034 | g0283 | EUR | GBR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00140 | hp1 | a0001 | c0001 | t0027 | g0118 | EUR | GBR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00140 | hp2 | a0001 | c0001 | t0014 | g0005 | EUR | GBR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0041 | EUR | FIN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00323 | hp1 | a0001 | c0001 | t0056 | g0090 | EUR | FIN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00323 | hp2 | a0001 | c0001 | t0049 | g0152 | EUR | FIN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | CHS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00738 | hp1 | a0001 | c0001 | t0020 | g0084 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0276 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0287 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01071 | hp2 | a0001 | c0001 | t0021 | g0150 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01074 | hp1 | a0001 | c0001 | t0021 | g0129 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01099 | hp2 | a0001 | c0001 | t0027 | g0144 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0263 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0246 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01167 | hp1 | a0001 | c0001 | t0014 | g0022 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01168 | hp2 | a0001 | c0001 | t0025 | g0007 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0262 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01169 | hp2 | a0001 | c0001 | t0025 | g0007 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01192 | hp2 | a0001 | c0001 | t0021 | g0128 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0269 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0285 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01256 | hp2 | a0001 | c0001 | t0014 | g0117 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01257 | hp2 | a0001 | c0001 | t0020 | g0057 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01358 | hp2 | a0001 | c0001 | t0046 | g0142 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0271 | AMR | CLM | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01515 | hp1 | a0001 | c0001 | t0028 | g0172 | EUR | IBS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0132 | EUR | IBS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01517 | hp1 | a0001 | c0001 | t0014 | g0005 | EUR | IBS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01517 | hp2 | a0001 | c0001 | t0028 | g0073 | EUR | IBS | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01884 | hp1 | a0001 | c0001 | t0022 | g0197 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01884 | hp2 | a0001 | c0001 | t0050 | g0153 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0181 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01928 | hp1 | a0001 | c0001 | t0029 | g0214 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01928 | hp2 | a0001 | c0001 | t0021 | g0130 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01934 | hp1 | a0001 | c0001 | t0020 | g0087 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01975 | hp1 | a0001 | c0001 | t0017 | g0094 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0085 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02027 | hp1 | a0001 | c0001 | t0045 | g0228 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02055 | hp1 | a0001 | c0001 | t0010 | g0193 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02129 | hp1 | a0001 | c0001 | t0026 | g0216 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02145 | hp1 | a0001 | c0001 | t0054 | g0294 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02148 | hp2 | a0001 | c0001 | t0029 | g0213 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CDX | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02257 | hp1 | a0001 | c0001 | t0024 | g0164 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0244 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02258 | hp2 | a0001 | c0001 | t0015 | g0256 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0185 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0277 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02572 | hp2 | a0001 | c0001 | t0042 | g0291 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0280 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0282 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02615 | hp2 | a0001 | c0001 | t0032 | g0119 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02647 | hp2 | a0001 | c0001 | t0058 | g0188 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0049 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02717 | hp1 | a0001 | c0001 | t0025 | g0171 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02717 | hp2 | a0001 | c0001 | t0031 | g0122 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02723 | hp1 | a0001 | c0001 | t0018 | g0121 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02735 | hp2 | a0001 | c0001 | t0016 | g0024 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0162 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02818 | hp1 | a0001 | c0001 | t0037 | g0288 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02818 | hp2 | a0001 | c0001 | t0023 | g0260 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02886 | hp1 | a0001 | c0001 | t0033 | g0200 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02886 | hp2 | a0001 | c0001 | t0015 | g0258 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02895 | hp1 | a0001 | c0001 | t0018 | g0116 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0176 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02897 | hp1 | a0001 | c0001 | t0023 | g0023 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02897 | hp2 | a0001 | c0001 | t0018 | g0115 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02922 | hp1 | a0001 | c0001 | t0060 | g0261 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0264 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02976 | hp2 | a0001 | c0001 | t0023 | g0259 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0268 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03098 | hp2 | a0001 | c0001 | t0041 | g0251 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03130 | hp1 | a0001 | c0001 | t0024 | g0187 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03130 | hp2 | a0001 | c0001 | t0035 | g0281 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03139 | hp1 | a0001 | c0001 | t0022 | g0198 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03209 | hp1 | a0001 | c0001 | t0061 | g0182 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0265 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0186 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03486 | hp1 | a0001 | c0001 | t0012 | g0042 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0266 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03490 | hp1 | a0001 | c0001 | t0017 | g0051 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0273 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03491 | hp1 | a0001 | c0001 | t0016 | g0100 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0274 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03492 | hp1 | a0001 | c0001 | t0016 | g0099 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0010 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03516 | hp1 | a0001 | c0001 | t0022 | g0199 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0175 | AFR | ESN | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0178 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03579 | hp1 | a0001 | c0001 | t0051 | g0194 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03579 | hp2 | a0001 | c0001 | t0059 | g0295 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0138 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0270 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03704 | hp2 | a0001 | c0001 | t0017 | g0077 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03834 | hp2 | a0001 | c0001 | t0043 | g0157 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | STU | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG04184 | hp2 | a0001 | c0001 | t0016 | g0012 | SAS | BEB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG04199 | hp2 | a0001 | c0001 | t0039 | g0221 | SAS | STU | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | YRI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18522 | hp2 | a0001 | c0001 | t0053 | g0189 | AFR | YRI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18612 | hp1 | a0001 | c0001 | t0057 | g0014 | EAS | CHB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | CHB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | CHB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0278 | AFR | YRI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | YRI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18953 | hp2 | a0001 | c0001 | t0052 | g0113 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18957 | hp1 | a0001 | c0001 | t0030 | g0053 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18965 | hp1 | a0001 | c0001 | t0026 | g0029 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18972 | hp1 | a0001 | c0001 | t0038 | g0163 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18982 | hp2 | a0001 | c0001 | t0062 | g0019 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18989 | hp2 | a0001 | c0001 | t0019 | g0070 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19009 | hp1 | a0001 | c0001 | t0019 | g0063 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19011 | hp1 | a0001 | c0001 | t0019 | g0069 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | LWK | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19030 | hp2 | a0001 | c0001 | t0018 | g0120 | AFR | LWK | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | LWK | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0184 | AFR | LWK | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19083 | hp1 | a0001 | c0001 | t0017 | g0097 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19084 | hp2 | a0001 | c0001 | t0019 | g0076 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19091 | hp1 | a0001 | c0001 | t0055 | g0080 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | YRI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | YRI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0257 | AFR | ASW | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA20129 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | ASW | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0136 | EUR | TSI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA20752 | hp2 | a0001 | c0001 | t0040 | g0223 | EUR | TSI | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0192 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02486 | hp2 | a0001 | c0001 | t0044 | g0247 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02559 | hp1 | a0001 | c0001 | t0024 | g0190 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ACB | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0191 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG06807 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | USA | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | USA | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA20300 | hp1 | a0001 | c0001 | t0047 | g0165 | AFR | USA | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | USA | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | LWK | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
NA21309 | hp2 | a0001 | c0001 | t0015 | g0255 | AFR | LWK | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
homoSapiens | chm13v2 | a0001 | c0001 | t0036 | g0286 | REF | REF | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0179 | REF | REF | CREB1_chr2_207524962_207610988 | CREB1 | chr2 | 207524962 | 207610988 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:207597275 | G | A | 1 | a0001c0001t0030 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 217 | chr2 | 207597275 | ||||||
chr2:207597397 | A | T | 1 | a0001c0001t0021 | 4 | HG01071.hp2 HG01074.hp1 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*339A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 339 | chr2 | 207597397 | ||||||
chr2:207597867 | A | G | 1 | a0001c0001t0062 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*809A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 809 | chr2 | 207597867 | ||||||
chr2:207597888 | T | G | 2 | a0001c0001t0031 a0001c0001t0032 |
2 | HG02615.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*830T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 830 | chr2 | 207597888 | ||||||
chr2:207597980 | C | T | 1 | a0001c0001t0029 | 2 | HG01928.hp1 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*922C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 922 | chr2 | 207597980 | ||||||
chr2:207598255 | C | T | 1 | a0001c0001t0020 | 4 | HG00738.hp1 HG01257.hp2 HG01934.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1197C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1197 | chr2 | 207598255 | ||||||
chr2:207598486 | TAA | T | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*1443_*1444delAA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1443 | INFO_REALIGN_3_PRIME | chr2 | 207598486 | |||||
chr2:207598486 | TAAA | T | 5 | a0001c0001t0008 a0001c0001t0018 a0001c0001t0019 others(2): Show |
18 | HG01891.hp1 HG02723.hp1 HG02895.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1442_*1444delAAA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr2 | 207598486 | |||||
chr2:207598569 | G | A | 1 | a0001c0001t0012 | 5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1511G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1511 | chr2 | 207598569 | ||||||
chr2:207598617 | T | G | 1 | a0001c0001t0010 | 6 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1559T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1559 | chr2 | 207598617 | ||||||
chr2:207598698 | T | G | 1 | a0001c0001t0060 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1640T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1640 | chr2 | 207598698 | ||||||
chr2:207598729 | C | A | 2 | a0001c0001t0022 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1671C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1671 | chr2 | 207598729 | ||||||
chr2:207598796 | C | G | 1 | a0001c0001t0060 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1738C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1738 | chr2 | 207598796 | ||||||
chr2:207598820 | C | T | 1 | a0001c0001t0009 | 6 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1762C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1762 | chr2 | 207598820 | ||||||
chr2:207598850 | TA | T | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1800delA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1800 | INFO_REALIGN_3_PRIME | chr2 | 207598850 | |||||
chr2:207598900 | G | A | 1 | a0001c0001t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1842G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1842 | chr2 | 207598900 | ||||||
chr2:207598936 | A | G | 2 | a0001c0001t0022 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1878A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1878 | chr2 | 207598936 | ||||||
chr2:207598946 | G | A | 1 | a0001c0001t0038 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1888 | chr2 | 207598946 | ||||||
chr2:207598995 | G | A | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0026 others(8): Show |
65 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1937 | chr2 | 207598995 | ||||||
chr2:207599045 | T | C | 1 | a0001c0001t0039 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1987T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 1987 | chr2 | 207599045 | ||||||
chr2:207599067 | G | A | 1 | a0001c0001t0046 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 2009 | chr2 | 207599067 | ||||||
chr2:207599690 | G | C | 1 | a0001c0001t0046 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2632G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 2632 | chr2 | 207599690 | ||||||
chr2:207599843 | A | G | 1 | a0001c0001t0045 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2785A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 2785 | chr2 | 207599843 | ||||||
chr2:207600238 | C | CAT | 10 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0019 others(7): Show |
75 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3204_*3205dupTA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3206 | INFO_REALIGN_3_PRIME | chr2 | 207600238 | |||||
chr2:207600238 | C | CATAT | 7 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0030 others(4): Show |
11 | HG01515.hp1 HG01517.hp2 HG01975.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3202_*3205dupTATA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3206 | INFO_REALIGN_3_PRIME | chr2 | 207600238 | |||||
chr2:207600238 | CAT | C | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(23): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*3204_*3205delTA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3204 | INFO_REALIGN_3_PRIME | chr2 | 207600238 | |||||
chr2:207600238 | CATAT | C | 2 | a0001c0001t0014 a0001c0001t0022 |
7 | HG00140.hp2 HG01167.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3202_*3205delTATA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3202 | INFO_REALIGN_3_PRIME | chr2 | 207600238 | |||||
chr2:207600620 | C | T | 1 | a0001c0001t0042 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3562C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3562 | chr2 | 207600620 | ||||||
chr2:207600721 | A | G | 1 | a0001c0001t0060 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3663A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3663 | chr2 | 207600721 | ||||||
chr2:207600820 | C | T | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(3): Show |
28 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3762C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3762 | chr2 | 207600820 | ||||||
chr2:207600925 | T | C | 1 | a0001c0001t0015 | 4 | HG02258.hp2 HG02886.hp2 NA20129.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3867T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3867 | chr2 | 207600925 | ||||||
chr2:207600951 | C | A | 1 | a0001c0001t0051 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3893C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3893 | chr2 | 207600951 | ||||||
chr2:207600987 | GTC | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*3933_*3934delCT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3933 | INFO_REALIGN_3_PRIME | chr2 | 207600987 | |||||
chr2:207601054 | A | G | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*3996A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 3996 | chr2 | 207601054 | ||||||
chr2:207601124 | CTTTA | C | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*4070_*4073delATTT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 4070 | INFO_REALIGN_3_PRIME | chr2 | 207601124 | |||||
chr2:207601280 | G | C | 1 | a0001c0001t0052 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4222G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 4222 | chr2 | 207601280 | ||||||
chr2:207601546 | A | G | 3 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0034 |
19 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4488A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 4488 | chr2 | 207601546 | ||||||
chr2:207601642 | A | T | 12 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0023 others(9): Show |
68 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*4584A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 4584 | chr2 | 207601642 | ||||||
chr2:207601716 | G | T | 1 | a0001c0001t0056 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4658G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 4658 | chr2 | 207601716 | ||||||
chr2:207601729 | C | A | 1 | a0001c0001t0027 | 2 | HG00140.hp1 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4671C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 4671 | chr2 | 207601729 | ||||||
chr2:207602080 | T | C | 1 | a0001c0001t0040 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5022T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5022 | chr2 | 207602080 | ||||||
chr2:207602384 | A | C | 1 | a0001c0001t0055 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5326A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5326 | chr2 | 207602384 | ||||||
chr2:207602426 | A | G | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*5368A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5368 | chr2 | 207602426 | ||||||
chr2:207602475 | T | A | 1 | a0001c0001t0041 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5417T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5417 | chr2 | 207602475 | ||||||
chr2:207602476 | T | C | 1 | a0001c0001t0041 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5418T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5418 | chr2 | 207602476 | ||||||
chr2:207602549 | G | A | 2 | a0001c0001t0022 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5491G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5491 | chr2 | 207602549 | ||||||
chr2:207602864 | T | C | 1 | a0001c0001t0047 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5806T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5806 | chr2 | 207602864 | ||||||
chr2:207602887 | C | T | 1 | a0001c0001t0050 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5829C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5829 | chr2 | 207602887 | ||||||
chr2:207603035 | C | T | 1 | a0001c0001t0028 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5977C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 5977 | chr2 | 207603035 | ||||||
chr2:207603073 | T | G | 1 | a0001c0001t0048 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6015T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6015 | chr2 | 207603073 | ||||||
chr2:207603088 | T | C | 1 | a0001c0001t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6030T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6030 | chr2 | 207603088 | ||||||
chr2:207603273 | A | G | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*6215A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6215 | chr2 | 207603273 | ||||||
chr2:207603465 | A | G | 2 | a0001c0001t0054 a0001c0001t0059 |
2 | HG02145.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6407A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6407 | chr2 | 207603465 | ||||||
chr2:207603724 | G | A | 1 | a0001c0001t0026 | 2 | HG02129.hp1 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6666G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6666 | chr2 | 207603724 | ||||||
chr2:207603748 | C | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*6690C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6690 | chr2 | 207603748 | ||||||
chr2:207604040 | T | C | 1 | a0001c0001t0016 | 4 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6982T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 6982 | chr2 | 207604040 | ||||||
chr2:207604087 | C | T | 3 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0034 |
19 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7029C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7029 | chr2 | 207604087 | ||||||
chr2:207604215 | A | G | 1 | a0001c0001t0060 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7157A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7157 | chr2 | 207604215 | ||||||
chr2:207604321 | C | A | 2 | a0001c0001t0007 a0001c0001t0044 |
10 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7263C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7263 | chr2 | 207604321 | ||||||
chr2:207604401 | T | G | 1 | a0001c0001t0012 | 5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7343T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7343 | chr2 | 207604401 | ||||||
chr2:207604460 | T | C | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*7402T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7402 | chr2 | 207604460 | ||||||
chr2:207604489 | ATCTT | A | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*7436_*7439delTCTT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7436 | INFO_REALIGN_3_PRIME | chr2 | 207604489 | |||||
chr2:207604579 | A | T | 1 | a0001c0001t0025 | 3 | HG01168.hp2 HG01169.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7521A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7521 | chr2 | 207604579 | ||||||
chr2:207604670 | AACC | A | 2 | a0001c0001t0022 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7618_*7620delCAC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7618 | INFO_REALIGN_3_PRIME | chr2 | 207604670 | |||||
chr2:207604675 | C | T | 1 | a0001c0001t0049 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7617C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7617 | chr2 | 207604675 | ||||||
chr2:207604778 | T | G | 1 | a0001c0001t0012 | 5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7720T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7720 | chr2 | 207604778 | ||||||
chr2:207604861 | T | C | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*7803T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 7803 | chr2 | 207604861 | ||||||
chr2:207605283 | G | A | 1 | a0001c0001t0034 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8225G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 8225 | chr2 | 207605283 | ||||||
chr2:207605571 | GTGTTA | G | 8 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0011 others(5): Show |
27 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*8518_*8522delATGT others(1): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 8518 | INFO_REALIGN_3_PRIME | chr2 | 207605571 | |||||
chr2:207605724 | C | T | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*8666C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 8/8 | 8666 | chr2 | 207605724 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:207530187 | G | A | 1 | a0001c0001t0003g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-9+53G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530187 | |||||||
chr2:207530194 | C | A | 1 | a0001c0001t0016g0012 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-9+60C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530194 | |||||||
chr2:207530438 | T | A | 2 | a0001c0001t0004g0013 a0001c0001t0057g0014 |
2 | NA18612.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-9+304T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530438 | |||||||
chr2:207530525 | G | A | 1 | a0001c0001t0003g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9+391G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530525 | |||||||
chr2:207530543 | C | T | 3 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 |
3 | HG02145.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-9+409C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530543 | |||||||
chr2:207530589 | C | T | 1 | a0001c0001t0003g0293 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-9+455C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530589 | |||||||
chr2:207530607 | C | G | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9+473C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530607 | |||||||
chr2:207530865 | C | G | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0042g0291 |
3 | HG02572.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+731C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207530865 | |||||||
chr2:207530970 | CT | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(14): Show |
17 | HG01070.hp1 HG01167.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9+851delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207530970 | ||||||
chr2:207531221 | C | A | 1 | a0001c0001t0001g0033 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-9+1087C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207531221 | |||||||
chr2:207531345 | A | G | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+1211A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207531345 | |||||||
chr2:207531463 | A | G | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+1329A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207531463 | |||||||
chr2:207531580 | C | T | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+1446C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207531580 | |||||||
chr2:207531674 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-9+1540G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207531674 | |||||||
chr2:207531831 | C | G | 1 | a0001c0001t0003g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9+1697C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207531831 | |||||||
chr2:207532346 | A | C | 4 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2212A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207532346 | |||||||
chr2:207533086 | C | CT | 32 | a0001c0001t0005g0031 a0001c0001t0005g0272 a0001c0001t0005g0274 others(29): Show |
33 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-9+2965dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207533086 | ||||||
chr2:207533088 | T | C | 4 | a0001c0001t0007g0003 a0001c0001t0007g0035 a0001c0001t0007g0036 others(1): Show |
5 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2954T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207533088 | |||||||
chr2:207533213 | A | AT | 83 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(80): Show |
86 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.-9+3089dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207533213 | ||||||
chr2:207533366 | C | G | 3 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 |
3 | HG02602.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-9+3232C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207533366 | |||||||
chr2:207533630 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-9+3496G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207533630 | |||||||
chr2:207533761 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18944.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-9+3627C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207533761 | |||||||
chr2:207533961 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | NA18946.hp2 NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-9+3827A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207533961 | |||||||
chr2:207534205 | A | G | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+4071A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207534205 | |||||||
chr2:207534476 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9+4342C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207534476 | |||||||
chr2:207534477 | G | T | 1 | a0001c0001t0003g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9+4343G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207534477 | |||||||
chr2:207534482 | C | G | 1 | a0001c0001t0003g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-9+4348C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207534482 | |||||||
chr2:207534962 | A | G | 2 | a0001c0001t0037g0288 a0001c0001t0041g0251 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+4828A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207534962 | |||||||
chr2:207534971 | C | T | 1 | a0001c0001t0012g0009 | 2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9+4837C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207534971 | |||||||
chr2:207535032 | A | G | 1 | a0001c0001t0057g0014 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-9+4898A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207535032 | |||||||
chr2:207535439 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9+5305A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207535439 | |||||||
chr2:207535620 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-9+5486A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207535620 | |||||||
chr2:207535643 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0003g0040 |
2 | NA18946.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-9+5509T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207535643 | |||||||
chr2:207535745 | C | CT | 6 | a0001c0001t0004g0195 a0001c0001t0008g0196 a0001c0001t0022g0197 others(3): Show |
6 | HG00558.hp2 HG01884.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+5621dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207535745 | ||||||
chr2:207535794 | T | TTTTA | 259 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-9+5684_-9+5687dup others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207535794 | ||||||
chr2:207535794 | T | TTTTATTT others(1): Show |
5 | a0001c0001t0003g0041 a0001c0001t0012g0009 a0001c0001t0012g0042 others(2): Show |
6 | HG00280.hp2 HG03195.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+5680_-9+5687dup others(8): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207535794 | ||||||
chr2:207535964 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-9+5830G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207535964 | |||||||
chr2:207536009 | C | T | 3 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 |
3 | HG02145.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-9+5875C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536009 | |||||||
chr2:207536151 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-9+6017A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536151 | |||||||
chr2:207536214 | A | G | 1 | a0001c0001t0028g0172 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-9+6080A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536214 | |||||||
chr2:207536492 | T | G | 2 | a0001c0001t0003g0045 a0001c0001t0003g0046 |
2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-9+6358T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536492 | |||||||
chr2:207536542 | C | A | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+6408C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536542 | |||||||
chr2:207536589 | G | A | 1 | a0001c0001t0054g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9+6455G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536589 | |||||||
chr2:207536590 | T | G | 1 | a0001c0001t0003g0048 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-9+6456T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536590 | |||||||
chr2:207536728 | G | A | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-9+6594G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536728 | |||||||
chr2:207536739 | C | T | 1 | a0001c0001t0003g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-9+6605C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207536739 | |||||||
chr2:207537053 | TTTG | T | 256 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(253): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.-9+6938_-9+6940del others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207537053 | ||||||
chr2:207537160 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-9+7026T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537160 | |||||||
chr2:207537507 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9+7373G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537507 | |||||||
chr2:207537539 | G | T | 1 | a0001c0001t0038g0163 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-9+7405G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537539 | |||||||
chr2:207537587 | T | C | 1 | a0001c0001t0004g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-9+7453T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537587 | |||||||
chr2:207537736 | A | G | 1 | a0001c0001t0016g0024 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-9+7602A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537736 | |||||||
chr2:207537833 | A | G | 1 | a0001c0001t0012g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9+7699A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537833 | |||||||
chr2:207537867 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-9+7733T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207537867 | |||||||
chr2:207538011 | T | A | 1 | a0001c0001t0038g0163 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-9+7877T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207538011 | |||||||
chr2:207538026 | T | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
92 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-9+7892T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207538026 | |||||||
chr2:207538165 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9+8031C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207538165 | |||||||
chr2:207538808 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0004g0111 others(2): Show |
5 | NA18953.hp2 NA18964.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+8674A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207538808 | |||||||
chr2:207539044 | C | CT | 239 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(236): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-9+8925dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207539044 | ||||||
chr2:207539044 | C | CTT | 19 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0104 others(16): Show |
20 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+8924_-9+8925dup others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207539044 | ||||||
chr2:207539207 | A | AT | 78 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0204 others(75): Show |
82 | HG00642.hp1 HG01109.hp2 HG01346.hp2 others(79): Show |
intron_variant | MODIFIER | c.-9+9091dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207539207 | ||||||
chr2:207539274 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9+9140G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539274 | |||||||
chr2:207539313 | G | A | 1 | a0001c0001t0013g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9+9179G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539313 | |||||||
chr2:207539427 | C | T | 1 | a0001c0001t0007g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9+9293C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539427 | |||||||
chr2:207539631 | G | A | 2 | a0001c0001t0029g0213 a0001c0001t0029g0214 |
2 | HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-9+9497G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539631 | |||||||
chr2:207539817 | G | A | 2 | a0001c0001t0018g0115 a0001c0001t0018g0116 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-9+9683G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539817 | |||||||
chr2:207539855 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-9+9721C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539855 | |||||||
chr2:207539911 | A | G | 2 | a0001c0001t0003g0011 a0001c0001t0003g0156 |
2 | HG00558.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-9+9777A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539911 | |||||||
chr2:207539947 | A | G | 2 | a0001c0001t0016g0099 a0001c0001t0016g0100 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-9+9813A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207539947 | |||||||
chr2:207540113 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-9+9979A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540113 | |||||||
chr2:207540285 | A | G | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+10151A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540285 | |||||||
chr2:207540316 | GGCTAACG others(429): Show |
G | 1 | a0001c0001t0014g0117 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-9+10183_-9+10618d others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540316 | |||||||
chr2:207540322 | C | T | 1 | a0001c0001t0019g0069 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-9+10188C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540322 | |||||||
chr2:207540539 | G | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(62): Show |
68 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(65): Show |
intron_variant | MODIFIER | c.-9+10405G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540539 | |||||||
chr2:207540606 | G | C | 1 | a0001c0001t0048g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-9+10472G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540606 | |||||||
chr2:207540635 | A | G | 1 | a0001c0001t0024g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-9+10501A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540635 | |||||||
chr2:207540669 | T | TA | 16 | a0001c0001t0001g0168 a0001c0001t0002g0222 a0001c0001t0004g0025 others(13): Show |
17 | HG00099.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+10563dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207540669 | ||||||
chr2:207540669 | TA | T | 81 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(78): Show |
86 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.-9+10563delA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207540669 | ||||||
chr2:207540669 | TAA | T | 71 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0068 others(68): Show |
72 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-9+10562_-9+10563d others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207540669 | ||||||
chr2:207540669 | TAAA | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(76): Show |
80 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-9+10561_-9+10563d others(5): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207540669 | ||||||
chr2:207540669 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0008g0001 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+10554_-9+10563d others(12): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207540669 | ||||||
chr2:207540753 | T | A | 1 | a0001c0001t0014g0117 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-9+10619T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540753 | |||||||
chr2:207540754 | T | G | 1 | a0001c0001t0014g0117 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-9+10620T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540754 | |||||||
chr2:207540958 | A | G | 260 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(257): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-9+10824A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207540958 | |||||||
chr2:207541168 | G | A | 131 | a0001c0001t0001g0039 a0001c0001t0001g0147 a0001c0001t0002g0002 others(128): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-9+11034G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207541168 | |||||||
chr2:207541368 | G | A | 1 | a0001c0001t0003g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-9+11234G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207541368 | |||||||
chr2:207541741 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-9+11607G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207541741 | |||||||
chr2:207541827 | A | C | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-9+11693A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207541827 | |||||||
chr2:207542167 | T | C | 1 | a0001c0001t0023g0023 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-9+12033T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207542167 | |||||||
chr2:207542207 | A | G | 4 | a0001c0001t0015g0255 a0001c0001t0015g0256 a0001c0001t0015g0257 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+12073A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207542207 | |||||||
chr2:207542445 | G | T | 1 | a0001c0001t0002g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9+12311G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207542445 | |||||||
chr2:207542537 | A | T | 1 | a0001c0001t0003g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-9+12403A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207542537 | |||||||
chr2:207542757 | T | C | 1 | a0001c0001t0017g0051 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9+12623T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207542757 | |||||||
chr2:207542823 | C | T | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+12689C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207542823 | |||||||
chr2:207543092 | A | T | 8 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(5): Show |
9 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-12536A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543092 | |||||||
chr2:207543169 | G | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(120): Show |
125 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-8-12459G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543169 | |||||||
chr2:207543170 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8-12458C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543170 | |||||||
chr2:207543511 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8-12117A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543511 | |||||||
chr2:207543680 | G | T | 1 | a0001c0001t0003g0154 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8-11948G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543680 | |||||||
chr2:207543825 | G | A | 1 | a0001c0001t0027g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-8-11803G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543825 | |||||||
chr2:207543847 | C | G | 3 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 |
3 | HG02145.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-8-11781C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543847 | |||||||
chr2:207543860 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-8-11768C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543860 | |||||||
chr2:207543986 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-8-11642C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207543986 | |||||||
chr2:207544005 | T | C | 1 | a0001c0001t0012g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-8-11623T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544005 | |||||||
chr2:207544015 | G | A | 4 | a0001c0001t0009g0264 a0001c0001t0009g0267 a0001c0001t0009g0268 others(1): Show |
4 | HG01243.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-11613G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544015 | |||||||
chr2:207544024 | A | G | 131 | a0001c0001t0001g0039 a0001c0001t0001g0108 a0001c0001t0001g0109 others(128): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-8-11604A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544024 | |||||||
chr2:207544227 | A | G | 1 | a0001c0001t0024g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-11401A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544227 | |||||||
chr2:207544533 | G | A | 3 | a0001c0001t0015g0255 a0001c0001t0015g0256 a0001c0001t0015g0257 |
3 | HG02258.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-8-11095G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544533 | |||||||
chr2:207544615 | G | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
92 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-8-11013G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544615 | |||||||
chr2:207544759 | A | G | 1 | a0001c0001t0006g0285 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-8-10869A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544759 | |||||||
chr2:207544764 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-8-10864C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544764 | |||||||
chr2:207544933 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-8-10695G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207544933 | |||||||
chr2:207545380 | G | C | 1 | a0001c0001t0030g0053 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-8-10248G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207545380 | |||||||
chr2:207545543 | T | C | 30 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0005g0031 others(27): Show |
31 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-10085T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207545543 | |||||||
chr2:207545731 | C | CT | 10 | a0001c0001t0002g0209 a0001c0001t0007g0003 a0001c0001t0007g0035 others(7): Show |
11 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-9880dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207545731 | ||||||
chr2:207545731 | CT | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(118): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-8-9880delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207545731 | ||||||
chr2:207545764 | G | A | 2 | a0001c0001t0003g0154 a0001c0001t0003g0161 |
2 | HG02015.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-8-9864G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207545764 | |||||||
chr2:207545787 | G | A | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-9841G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207545787 | |||||||
chr2:207545844 | C | T | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(280): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-8-9784C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207545844 | |||||||
chr2:207545858 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-8-9770C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207545858 | |||||||
chr2:207546025 | G | A | 1 | a0001c0001t0043g0157 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-8-9603G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546025 | |||||||
chr2:207546053 | C | T | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8-9575C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546053 | |||||||
chr2:207546265 | T | C | 1 | a0001c0001t0041g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-9363T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546265 | |||||||
chr2:207546476 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8-9152C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546476 | |||||||
chr2:207546542 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-8-9086C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546542 | |||||||
chr2:207546564 | T | TA | 6 | a0001c0001t0010g0026 a0001c0001t0010g0183 a0001c0001t0010g0184 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-9059dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207546564 | ||||||
chr2:207546579 | T | C | 10 | a0001c0001t0001g0168 a0001c0001t0003g0296 a0001c0001t0004g0025 others(7): Show |
11 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-9049T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546579 | |||||||
chr2:207546588 | G | T | 2 | a0001c0001t0005g0284 a0001c0001t0034g0283 |
2 | HG00099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-8-9040G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546588 | |||||||
chr2:207546690 | C | A | 1 | a0001c0001t0032g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8-8938C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546690 | |||||||
chr2:207546728 | C | CA | 98 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(95): Show |
100 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-8-8890dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207546728 | ||||||
chr2:207546932 | T | C | 6 | a0001c0001t0007g0003 a0001c0001t0007g0035 a0001c0001t0007g0036 others(3): Show |
7 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-8696T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546932 | |||||||
chr2:207546950 | A | T | 1 | a0001c0001t0033g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-8678A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207546950 | |||||||
chr2:207547243 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-8385A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207547243 | |||||||
chr2:207547368 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-8260C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207547368 | |||||||
chr2:207547391 | G | C | 4 | a0001c0001t0018g0115 a0001c0001t0018g0116 a0001c0001t0018g0120 others(1): Show |
4 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-8237G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207547391 | |||||||
chr2:207547808 | A | G | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-7820A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207547808 | |||||||
chr2:207547862 | G | A | 1 | a0001c0001t0011g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-8-7766G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207547862 | |||||||
chr2:207547946 | A | G | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-8-7682A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207547946 | |||||||
chr2:207548123 | G | A | 12 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(9): Show |
13 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-7505G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548123 | |||||||
chr2:207548124 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | NA18946.hp2 NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-8-7504G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548124 | |||||||
chr2:207548151 | G | A | 2 | a0001c0001t0002g0210 a0001c0001t0002g0218 |
2 | HG02155.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-8-7477G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548151 | |||||||
chr2:207548158 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-8-7470G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548158 | |||||||
chr2:207548196 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-7432A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548196 | |||||||
chr2:207548246 | A | T | 1 | a0001c0001t0015g0257 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-7382A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548246 | |||||||
chr2:207548523 | G | T | 2 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
2 | NA18944.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.-8-7105G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548523 | |||||||
chr2:207548773 | C | A | 30 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(27): Show |
31 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-6855C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548773 | |||||||
chr2:207548775 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8-6853A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548775 | |||||||
chr2:207548915 | T | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | NA18946.hp2 NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-8-6713T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207548915 | |||||||
chr2:207549024 | G | C | 1 | a0001c0001t0003g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-8-6604G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207549024 | |||||||
chr2:207549413 | T | C | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-8-6215T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207549413 | |||||||
chr2:207549568 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-8-6060G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207549568 | |||||||
chr2:207549670 | C | T | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5958C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207549670 | |||||||
chr2:207549728 | A | T | 1 | a0001c0001t0049g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8-5900A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207549728 | |||||||
chr2:207549749 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-8-5879G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207549749 | |||||||
chr2:207550169 | G | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0035 a0001c0001t0007g0036 others(1): Show |
5 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-5459G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550169 | |||||||
chr2:207550176 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0289 a0001c0001t0002g0290 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-5452A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550176 | |||||||
chr2:207550198 | C | T | 1 | a0001c0001t0002g0239 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-8-5430C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550198 | |||||||
chr2:207550235 | A | T | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-5393A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550235 | |||||||
chr2:207550333 | C | CT | 34 | a0001c0001t0001g0098 a0001c0001t0003g0296 a0001c0001t0004g0292 others(31): Show |
35 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-8-5276dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207550333 | ||||||
chr2:207550333 | CT | C | 17 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0202 others(14): Show |
17 | HG00558.hp1 HG01167.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-5276delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207550333 | ||||||
chr2:207550413 | A | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(253): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.-8-5215A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550413 | |||||||
chr2:207550617 | C | T | 260 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(257): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.-8-5011C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550617 | |||||||
chr2:207550631 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8-4997A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207550631 | |||||||
chr2:207551096 | A | T | 5 | a0001c0001t0008g0001 a0001c0001t0008g0008 a0001c0001t0008g0181 others(2): Show |
8 | HG01891.hp1 HG02922.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-4532A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551096 | |||||||
chr2:207551263 | T | G | 1 | a0001c0001t0033g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-4365T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551263 | |||||||
chr2:207551761 | G | A | 1 | a0001c0001t0058g0188 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8-3867G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551761 | |||||||
chr2:207551903 | A | G | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3725A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551903 | |||||||
chr2:207551911 | G | A | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3717G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551911 | |||||||
chr2:207551922 | G | A | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3706G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551922 | |||||||
chr2:207551934 | C | T | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3694C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551934 | |||||||
chr2:207551935 | A | G | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3693A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551935 | |||||||
chr2:207551949 | A | G | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3679A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551949 | |||||||
chr2:207551953 | G | A | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-3675G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551953 | |||||||
chr2:207551997 | G | A | 1 | a0001c0001t0022g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-3631G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207551997 | |||||||
chr2:207552024 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0160 others(1): Show |
6 | NA18952.hp1 NA18962.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3604A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552024 | |||||||
chr2:207552042 | C | CA | 17 | a0001c0001t0002g0218 a0001c0001t0002g0236 a0001c0001t0002g0237 others(14): Show |
17 | HG00323.hp1 HG00323.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-3561dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207552042 | ||||||
chr2:207552042 | C | CAA | 149 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(146): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-8-3562_-8-3561dup others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207552042 | ||||||
chr2:207552042 | C | CAAA | 56 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0039 others(53): Show |
57 | HG00140.hp2 HG00642.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-8-3563_-8-3561dup others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207552042 | ||||||
chr2:207552042 | CA | C | 24 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(21): Show |
25 | HG00099.hp2 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-3561delA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207552042 | ||||||
chr2:207552237 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-3391A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552237 | |||||||
chr2:207552437 | G | A | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8-3191G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552437 | |||||||
chr2:207552524 | G | GTAT | 255 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(252): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.-8-3103_-8-3101dup others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207552524 | ||||||
chr2:207552577 | G | A | 1 | a0001c0001t0006g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-3051G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552577 | |||||||
chr2:207552606 | C | CT | 13 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0002g0002 others(10): Show |
16 | HG01346.hp1 HG02056.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8-3006dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207552606 | ||||||
chr2:207552669 | G | A | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-8-2959G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552669 | |||||||
chr2:207552675 | G | A | 128 | a0001c0001t0001g0039 a0001c0001t0001g0147 a0001c0001t0002g0002 others(125): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-8-2953G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552675 | |||||||
chr2:207552822 | G | C | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8-2806G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552822 | |||||||
chr2:207552876 | C | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(253): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.-8-2752C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207552876 | |||||||
chr2:207553062 | CT | C | 11 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(8): Show |
12 | HG00099.hp1 HG01081.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8-2542delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207553062 | ||||||
chr2:207553062 | CTT | C | 39 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0002g0002 others(36): Show |
42 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-2543_-8-2542del others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207553062 | ||||||
chr2:207553062 | CTTT | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(209): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-8-2544_-8-2542del others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207553062 | ||||||
chr2:207553122 | G | A | 1 | a0001c0001t0048g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-8-2506G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553122 | |||||||
chr2:207553213 | T | C | 34 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(31): Show |
36 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-8-2415T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553213 | |||||||
chr2:207553377 | C | T | 30 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(27): Show |
31 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-2251C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553377 | |||||||
chr2:207553504 | CAG | C | 23 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
23 | HG00438.hp1 HG00738.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8-2121_-8-2120del others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207553504 | ||||||
chr2:207553589 | A | G | 30 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(27): Show |
31 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-2039A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553589 | |||||||
chr2:207553608 | G | A | 34 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(31): Show |
36 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-8-2020G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553608 | |||||||
chr2:207553674 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0289 a0001c0001t0002g0290 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1954A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553674 | |||||||
chr2:207553707 | T | C | 1 | a0001c0001t0003g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-8-1921T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553707 | |||||||
chr2:207553771 | T | C | 1 | a0001c0001t0017g0077 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-1857T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553771 | |||||||
chr2:207553909 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0098 a0001c0001t0001g0205 others(2): Show |
5 | NA18944.hp1 NA18950.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1719G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553909 | |||||||
chr2:207553922 | A | T | 1 | a0001c0001t0005g0276 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-8-1706A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207553922 | |||||||
chr2:207554064 | T | C | 1 | a0001c0001t0003g0134 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-8-1564T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207554064 | |||||||
chr2:207554241 | A | G | 2 | a0001c0001t0031g0122 a0001c0001t0032g0119 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-8-1387A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207554241 | |||||||
chr2:207554281 | G | C | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-1347G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207554281 | |||||||
chr2:207554372 | A | G | 1 | a0001c0001t0059g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8-1256A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207554372 | |||||||
chr2:207554377 | C | T | 1 | a0001c0001t0034g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8-1251C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207554377 | |||||||
chr2:207555013 | T | A | 1 | a0001c0001t0040g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-8-615T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555013 | |||||||
chr2:207555102 | C | T | 1 | a0001c0001t0030g0053 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-8-526C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555102 | |||||||
chr2:207555123 | T | TCC | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-505_-8-504insCC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555123 | |||||||
chr2:207555124 | A | T | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-504A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555124 | |||||||
chr2:207555126 | T | C | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-502T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555126 | |||||||
chr2:207555161 | C | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0160 others(2): Show |
7 | NA18952.hp1 NA18962.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-467C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555161 | |||||||
chr2:207555164 | T | TC | 5 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0160 others(2): Show |
7 | NA18952.hp1 NA18962.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-463dupC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 207555164 | ||||||
chr2:207555395 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8-233C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555395 | |||||||
chr2:207555560 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8-68A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555560 | |||||||
chr2:207555578 | G | A | 1 | a0001c0001t0010g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8-50G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 1/7 | chr2 | 207555578 | |||||||
chr2:207555940 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+191A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207555940 | |||||||
chr2:207556067 | T | A | 1 | a0001c0001t0012g0009 | 2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.114+318T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207556067 | |||||||
chr2:207556253 | C | A | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.114+504C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207556253 | |||||||
chr2:207556431 | G | A | 3 | a0001c0001t0023g0023 a0001c0001t0023g0259 a0001c0001t0023g0260 |
3 | HG02818.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.114+682G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207556431 | |||||||
chr2:207556445 | A | C | 1 | a0001c0001t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+696A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207556445 | |||||||
chr2:207556632 | G | C | 1 | a0001c0001t0058g0188 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+883G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207556632 | |||||||
chr2:207556831 | T | C | 1 | a0001c0001t0009g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114+1082T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207556831 | |||||||
chr2:207557025 | G | A | 67 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(64): Show |
70 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(67): Show |
intron_variant | MODIFIER | c.114+1276G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207557025 | |||||||
chr2:207557457 | C | T | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.114+1708C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207557457 | |||||||
chr2:207557539 | G | A | 30 | a0001c0001t0002g0028 a0001c0001t0002g0236 a0001c0001t0005g0031 others(27): Show |
31 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.114+1790G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207557539 | |||||||
chr2:207557611 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.114+1862C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207557611 | |||||||
chr2:207557613 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.114+1864G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207557613 | |||||||
chr2:207558090 | G | T | 2 | a0001c0001t0019g0063 a0001c0001t0019g0076 |
2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.115-2136G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558090 | |||||||
chr2:207558275 | C | G | 1 | a0001c0001t0061g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-1951C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558275 | |||||||
chr2:207558643 | AT | A | 8 | a0001c0001t0001g0095 a0001c0001t0003g0296 a0001c0001t0004g0058 others(5): Show |
8 | HG01167.hp1 HG01256.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1565delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 207558643 | ||||||
chr2:207558673 | T | A | 1 | a0001c0001t0010g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.115-1553T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558673 | |||||||
chr2:207558705 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.115-1521C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558705 | |||||||
chr2:207558755 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115-1471C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558755 | |||||||
chr2:207558906 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0064 |
3 | NA18991.hp2 NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.115-1320G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558906 | |||||||
chr2:207558955 | T | A | 2 | a0001c0001t0004g0065 a0001c0001t0017g0051 |
2 | HG01243.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.115-1271T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207558955 | |||||||
chr2:207559738 | G | A | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.115-488G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207559738 | |||||||
chr2:207559823 | G | A | 11 | a0001c0001t0010g0026 a0001c0001t0010g0183 a0001c0001t0010g0184 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-403G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207559823 | |||||||
chr2:207560071 | A | T | 1 | a0001c0001t0035g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-155A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207560071 | |||||||
chr2:207560074 | A | T | 1 | a0001c0001t0035g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-152A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207560074 | |||||||
chr2:207560099 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.115-127A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 2/7 | chr2 | 207560099 | |||||||
chr2:207560717 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0289 a0001c0001t0002g0290 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+345A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207560717 | |||||||
chr2:207560739 | T | A | 269 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(266): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.261+367T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207560739 | |||||||
chr2:207561533 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(91): Show |
96 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.261+1161G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207561533 | |||||||
chr2:207561544 | G | A | 1 | a0001c0001t0009g0264 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.261+1172G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207561544 | |||||||
chr2:207561835 | G | C | 1 | a0001c0001t0006g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.261+1463G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207561835 | |||||||
chr2:207562022 | A | G | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261+1650A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562022 | |||||||
chr2:207562074 | T | G | 126 | a0001c0001t0001g0039 a0001c0001t0001g0147 a0001c0001t0002g0002 others(123): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.261+1702T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562074 | |||||||
chr2:207562168 | C | A | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.261+1796C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562168 | |||||||
chr2:207562245 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+1873A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562245 | |||||||
chr2:207562490 | T | G | 1 | a0001c0001t0006g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.261+2118T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562490 | |||||||
chr2:207562500 | C | T | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261+2128C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562500 | |||||||
chr2:207562591 | C | G | 2 | a0001c0001t0002g0234 a0001c0001t0002g0237 |
2 | NA18986.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.261+2219C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562591 | |||||||
chr2:207562935 | A | G | 1 | a0001c0001t0006g0280 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.261+2563A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207562935 | |||||||
chr2:207563032 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.261+2660C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563032 | |||||||
chr2:207563108 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.261+2736G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563108 | |||||||
chr2:207563203 | G | C | 1 | a0001c0001t0002g0219 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.261+2831G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563203 | |||||||
chr2:207563213 | A | C | 4 | a0001c0001t0002g0242 a0001c0001t0002g0289 a0001c0001t0002g0290 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+2841A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563213 | |||||||
chr2:207563247 | A | G | 1 | a0001c0001t0023g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.261+2875A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563247 | |||||||
chr2:207563263 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+2891A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563263 | |||||||
chr2:207563344 | C | G | 3 | a0001c0001t0007g0003 a0001c0001t0007g0035 a0001c0001t0007g0037 |
4 | HG02109.hp2 HG02280.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+2972C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563344 | |||||||
chr2:207563647 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18944.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.261+3275T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563647 | |||||||
chr2:207563779 | A | T | 3 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 |
4 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+3407A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563779 | |||||||
chr2:207563805 | G | A | 1 | a0001c0001t0032g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.261+3433G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563805 | |||||||
chr2:207563837 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0056 |
2 | NA18948.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.261+3465G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563837 | |||||||
chr2:207563845 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.261+3473A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563845 | |||||||
chr2:207563852 | G | C | 1 | a0001c0001t0003g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.261+3480G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563852 | |||||||
chr2:207563859 | A | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(280): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.261+3487A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563859 | |||||||
chr2:207563877 | G | C | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.261+3505G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563877 | |||||||
chr2:207563884 | C | T | 10 | a0001c0001t0003g0006 a0001c0001t0003g0140 a0001c0001t0003g0141 others(7): Show |
11 | HG00140.hp1 HG01099.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.261+3512C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207563884 | |||||||
chr2:207564010 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(5): Show |
9 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.262-3453A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564010 | |||||||
chr2:207564093 | G | A | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-3370G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564093 | |||||||
chr2:207564211 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.262-3252T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564211 | |||||||
chr2:207564315 | C | T | 1 | a0001c0001t0035g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-3148C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564315 | |||||||
chr2:207564435 | T | C | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.262-3028T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564435 | |||||||
chr2:207564484 | C | T | 2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | NA19011.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.262-2979C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564484 | |||||||
chr2:207564510 | T | TA | 31 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(28): Show |
32 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.262-2941dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 207564510 | ||||||
chr2:207564535 | A | T | 1 | a0001c0001t0058g0188 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.262-2928A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564535 | |||||||
chr2:207564561 | A | G | 2 | a0001c0001t0003g0011 a0001c0001t0003g0156 |
2 | HG00558.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.262-2902A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564561 | |||||||
chr2:207564614 | A | G | 1 | a0001c0001t0022g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.262-2849A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564614 | |||||||
chr2:207564618 | A | G | 60 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(57): Show |
63 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(60): Show |
intron_variant | MODIFIER | c.262-2845A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564618 | |||||||
chr2:207564627 | T | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
92 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.262-2836T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564627 | |||||||
chr2:207564700 | C | T | 1 | a0001c0001t0010g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.262-2763C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564700 | |||||||
chr2:207564884 | A | T | 2 | a0001c0001t0022g0198 a0001c0001t0022g0199 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.262-2579A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207564884 | |||||||
chr2:207565038 | GT | G | 30 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(27): Show |
31 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.262-2412delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 207565038 | ||||||
chr2:207565164 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-2299A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565164 | |||||||
chr2:207565165 | C | T | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0211 others(2): Show |
5 | NA18964.hp1 NA18977.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-2298C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565165 | |||||||
chr2:207565365 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.262-2098G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565365 | |||||||
chr2:207565461 | A | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0089 a0001c0001t0004g0058 |
3 | HG01256.hp1 HG01346.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.262-2002A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565461 | |||||||
chr2:207565547 | A | G | 2 | a0001c0001t0002g0229 a0001c0001t0045g0228 |
2 | HG02027.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.262-1916A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565547 | |||||||
chr2:207565564 | A | C | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.262-1899A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565564 | |||||||
chr2:207565652 | G | T | 1 | a0001c0001t0041g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-1811G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565652 | |||||||
chr2:207565659 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.262-1804C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565659 | |||||||
chr2:207565805 | A | C | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.262-1658A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565805 | |||||||
chr2:207565943 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.262-1520G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207565943 | |||||||
chr2:207566225 | A | G | 2 | a0001c0001t0029g0213 a0001c0001t0029g0214 |
2 | HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.262-1238A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207566225 | |||||||
chr2:207566350 | T | G | 1 | a0001c0001t0035g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-1113T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207566350 | |||||||
chr2:207566464 | C | T | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-999C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207566464 | |||||||
chr2:207566554 | A | G | 2 | a0001c0001t0029g0213 a0001c0001t0029g0214 |
2 | HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.262-909A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207566554 | |||||||
chr2:207566648 | A | G | 6 | a0001c0001t0003g0131 a0001c0001t0003g0133 a0001c0001t0003g0148 others(3): Show |
7 | HG00140.hp2 HG01257.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-815A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207566648 | |||||||
chr2:207567009 | G | GA | 12 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0034 others(9): Show |
12 | HG01952.hp1 HG01993.hp1 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.262-453dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 207567009 | ||||||
chr2:207567016 | C | T | 8 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(5): Show |
9 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.262-447C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567016 | |||||||
chr2:207567041 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.262-422A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567041 | |||||||
chr2:207567088 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.262-375C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567088 | |||||||
chr2:207567106 | C | G | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.262-357C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567106 | |||||||
chr2:207567139 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.262-324T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567139 | |||||||
chr2:207567198 | G | T | 1 | a0001c0001t0005g0276 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.262-265G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567198 | |||||||
chr2:207567235 | C | G | 2 | a0001c0001t0007g0246 a0001c0001t0044g0247 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.262-228C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567235 | |||||||
chr2:207567274 | A | G | 1 | a0001c0001t0040g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.262-189A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567274 | |||||||
chr2:207567386 | AC | A | 4 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-76delC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 3/7 | chr2 | 207567386 | |||||||
chr2:207567622 | A | G | 8 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(5): Show |
9 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.362+59A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207567622 | |||||||
chr2:207568128 | A | T | 2 | a0001c0001t0007g0246 a0001c0001t0044g0247 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.362+565A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207568128 | |||||||
chr2:207568254 | G | A | 3 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 |
3 | HG02145.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.362+691G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207568254 | |||||||
chr2:207568339 | C | T | 1 | a0001c0001t0024g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.362+776C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207568339 | |||||||
chr2:207568520 | GC | G | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.362+959delC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 207568520 | ||||||
chr2:207568532 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.362+969A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207568532 | |||||||
chr2:207568839 | A | AT | 7 | a0001c0001t0010g0026 a0001c0001t0010g0183 a0001c0001t0010g0184 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+1285dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 207568839 | ||||||
chr2:207569030 | G | GATAC | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.363-1146_363-1143d others(6): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 207569030 | ||||||
chr2:207569050 | T | C | 1 | a0001c0001t0016g0012 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.363-1129T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569050 | |||||||
chr2:207569199 | A | G | 1 | a0001c0001t0010g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.363-980A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569199 | |||||||
chr2:207569273 | T | G | 1 | a0001c0001t0002g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.363-906T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569273 | |||||||
chr2:207569479 | G | A | 3 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 |
3 | HG02602.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.363-700G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569479 | |||||||
chr2:207569614 | C | G | 1 | a0001c0001t0059g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363-565C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569614 | |||||||
chr2:207569692 | T | C | 2 | a0001c0001t0003g0123 a0001c0001t0003g0127 |
2 | HG02273.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.363-487T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569692 | |||||||
chr2:207569729 | A | G | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.363-450A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569729 | |||||||
chr2:207569802 | G | A | 1 | a0001c0001t0004g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.363-377G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569802 | |||||||
chr2:207569921 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.363-258C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207569921 | |||||||
chr2:207570040 | C | CA | 49 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(46): Show |
50 | HG00738.hp1 HG01106.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.363-117dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 207570040 | ||||||
chr2:207570043 | A | C | 3 | a0001c0001t0003g0124 a0001c0001t0003g0139 a0001c0001t0003g0155 |
3 | NA18612.hp2 NA18960.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.363-136A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 4/7 | chr2 | 207570043 | |||||||
chr2:207570742 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.505+421C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207570742 | |||||||
chr2:207570798 | C | A | 1 | a0001c0001t0005g0284 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.505+477C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207570798 | |||||||
chr2:207570831 | T | C | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.505+510T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207570831 | |||||||
chr2:207570879 | A | G | 2 | a0001c0001t0007g0244 a0001c0001t0007g0245 |
2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.505+558A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207570879 | |||||||
chr2:207571022 | C | CTTTT | 5 | a0001c0001t0001g0059 a0001c0001t0012g0009 a0001c0001t0012g0042 others(2): Show |
6 | HG01496.hp1 HG03195.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+710_505+713dup others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207571022 | ||||||
chr2:207571022 | C | CTTTTTTT others(3): Show |
26 | a0001c0001t0001g0050 a0001c0001t0001g0060 a0001c0001t0001g0089 others(23): Show |
27 | HG00140.hp2 HG00673.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.505+704_505+713dup others(10): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207571022 | ||||||
chr2:207571022 | C | CTTTTTTT others(4): Show |
186 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(183): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.505+703_505+713dup others(11): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207571022 | ||||||
chr2:207571022 | C | CTTTTTTT others(5): Show |
33 | a0001c0001t0001g0020 a0001c0001t0002g0224 a0001c0001t0003g0146 others(30): Show |
34 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.505+702_505+713dup others(12): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207571022 | ||||||
chr2:207571167 | T | C | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.505+846T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571167 | |||||||
chr2:207571230 | C | A | 1 | a0001c0001t0004g0167 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.505+909C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571230 | |||||||
chr2:207571264 | C | T | 1 | a0001c0001t0025g0007 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.505+943C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571264 | |||||||
chr2:207571575 | C | T | 1 | a0001c0001t0049g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.505+1254C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571575 | |||||||
chr2:207571788 | A | T | 1 | a0001c0001t0010g0026 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.505+1467A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571788 | |||||||
chr2:207571895 | T | G | 4 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+1574T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571895 | |||||||
chr2:207571905 | C | T | 1 | a0001c0001t0003g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.505+1584C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571905 | |||||||
chr2:207571924 | AAATTGCT | A | 3 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 |
3 | HG02602.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.505+1605_505+1611d others(9): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207571924 | ||||||
chr2:207571958 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG01952.hp1 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+1637G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207571958 | |||||||
chr2:207572115 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.505+1794A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572115 | |||||||
chr2:207572225 | C | CA | 95 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(92): Show |
97 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.505+1922dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207572225 | ||||||
chr2:207572225 | CA | C | 11 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(8): Show |
12 | HG00099.hp1 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.505+1922delA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207572225 | ||||||
chr2:207572242 | A | G | 3 | a0001c0001t0003g0296 a0001c0001t0006g0010 a0001c0001t0006g0032 |
3 | HG01070.hp1 HG01071.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.505+1921A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572242 | |||||||
chr2:207572415 | A | T | 1 | a0001c0001t0002g0219 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.505+2094A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572415 | |||||||
chr2:207572616 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.505+2295A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572616 | |||||||
chr2:207572644 | G | A | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.505+2323G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572644 | |||||||
chr2:207572709 | G | A | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.505+2388G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572709 | |||||||
chr2:207572718 | A | G | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.505+2397A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572718 | |||||||
chr2:207572779 | G | A | 4 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(1): Show |
4 | NA18944.hp2 NA18948.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+2458G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572779 | |||||||
chr2:207572813 | C | CA | 6 | a0001c0001t0011g0176 a0001c0001t0011g0178 a0001c0001t0012g0009 others(3): Show |
7 | HG02895.hp2 HG03195.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-2445dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 207572813 | ||||||
chr2:207572964 | A | G | 5 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(2): Show |
5 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.506-2308A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207572964 | |||||||
chr2:207573586 | T | C | 1 | a0001c0001t0048g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.506-1686T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207573586 | |||||||
chr2:207573675 | G | T | 1 | a0001c0001t0016g0012 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.506-1597G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207573675 | |||||||
chr2:207573836 | A | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(253): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.506-1436A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207573836 | |||||||
chr2:207573878 | C | T | 4 | a0001c0001t0020g0057 a0001c0001t0020g0084 a0001c0001t0020g0085 others(1): Show |
4 | HG00738.hp1 HG01257.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-1394C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207573878 | |||||||
chr2:207574086 | A | G | 7 | a0001c0001t0002g0028 a0001c0001t0002g0227 a0001c0001t0002g0236 others(4): Show |
7 | NA18944.hp2 NA18948.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-1186A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207574086 | |||||||
chr2:207574290 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.506-982A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207574290 | |||||||
chr2:207574394 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(38): Show |
43 | HG00642.hp1 HG02027.hp1 HG02056.hp2 others(40): Show |
intron_variant | MODIFIER | c.506-878A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207574394 | |||||||
chr2:207574404 | G | T | 1 | a0001c0001t0010g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.506-868G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207574404 | |||||||
chr2:207574961 | G | A | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.506-311G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 5/7 | chr2 | 207574961 | |||||||
chr2:207575575 | C | G | 1 | a0001c0001t0003g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.688+121C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575575 | |||||||
chr2:207575622 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.688+168C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575622 | |||||||
chr2:207575668 | T | C | 1 | a0001c0001t0015g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.688+214T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575668 | |||||||
chr2:207575690 | T | C | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.688+236T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575690 | |||||||
chr2:207575741 | G | A | 4 | a0001c0001t0018g0115 a0001c0001t0018g0116 a0001c0001t0018g0120 others(1): Show |
4 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+287G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575741 | |||||||
chr2:207575899 | C | T | 60 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(57): Show |
63 | HG00642.hp1 HG01109.hp2 HG02027.hp1 others(60): Show |
intron_variant | MODIFIER | c.688+445C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575899 | |||||||
chr2:207575932 | CT | C | 5 | a0001c0001t0001g0168 a0001c0001t0004g0167 a0001c0001t0025g0007 others(2): Show |
6 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+480delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575932 | ||||||
chr2:207575934 | T | C | 4 | a0001c0001t0004g0025 a0001c0001t0004g0169 a0001c0001t0004g0170 others(1): Show |
4 | HG02809.hp1 HG02976.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+480T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575934 | |||||||
chr2:207575934 | T | TC | 40 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0160 others(37): Show |
45 | HG00140.hp1 HG00438.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.688+494dupC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575934 | ||||||
chr2:207575934 | T | TCC | 48 | a0001c0001t0001g0039 a0001c0001t0001g0078 a0001c0001t0001g0092 others(45): Show |
48 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.688+493_688+494dup others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575934 | ||||||
chr2:207575934 | T | TCCC | 35 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0002g0028 others(32): Show |
36 | HG00140.hp2 HG00642.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.688+492_688+494dup others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575934 | ||||||
chr2:207575934 | T | TCCCC | 18 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0001g0061 others(15): Show |
18 | HG00673.hp2 HG01167.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.688+491_688+494dup others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575934 | ||||||
chr2:207575934 | T | TCCCCC | 13 | a0001c0001t0001g0033 a0001c0001t0001g0082 a0001c0001t0002g0208 others(10): Show |
13 | HG01952.hp1 HG02027.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.688+490_688+494dup others(5): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575934 | ||||||
chr2:207575934 | T | TCCCCCCC others(4): Show |
2 | a0001c0001t0001g0083 a0001c0001t0002g0217 |
2 | HG02293.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.688+484_688+494dup others(11): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575934 | ||||||
chr2:207575946 | C | G | 1 | a0001c0001t0021g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.688+492C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575946 | |||||||
chr2:207575947 | C | CCCCT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0062 others(17): Show |
21 | HG00558.hp2 HG00673.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.688+494_688+495ins others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575947 | ||||||
chr2:207575947 | C | CCCT | 24 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0021 others(21): Show |
24 | HG00438.hp2 HG01081.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.688+494_688+495ins others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207575947 | ||||||
chr2:207575947 | C | CT | 5 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0174 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.688+493_688+494ins others(1): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575947 | |||||||
chr2:207575949 | A | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.688+495A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207575949 | |||||||
chr2:207576000 | A | T | 37 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0003g0040 others(34): Show |
39 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.688+546A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576000 | |||||||
chr2:207576003 | T | A | 4 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+549T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576003 | |||||||
chr2:207576063 | G | A | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.688+609G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576063 | |||||||
chr2:207576068 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.688+614C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576068 | |||||||
chr2:207576112 | G | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0088 others(2): Show |
5 | HG01070.hp2 HG01099.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.688+658G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576112 | |||||||
chr2:207576241 | C | CT | 8 | a0001c0001t0008g0001 a0001c0001t0008g0008 a0001c0001t0008g0181 others(5): Show |
11 | HG01891.hp1 HG02145.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.688+805dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207576241 | ||||||
chr2:207576241 | CT | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(208): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.688+805delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207576241 | ||||||
chr2:207576241 | CTT | C | 11 | a0001c0001t0001g0020 a0001c0001t0002g0173 a0001c0001t0002g0211 others(8): Show |
11 | HG00642.hp1 HG01074.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.688+804_688+805del others(2): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 207576241 | ||||||
chr2:207576266 | T | C | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.688+812T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576266 | |||||||
chr2:207576493 | A | C | 1 | a0001c0001t0002g0231 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.689-1012A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576493 | |||||||
chr2:207576932 | T | A | 1 | a0001c0001t0022g0198 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.689-573T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207576932 | |||||||
chr2:207577052 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.689-453C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207577052 | |||||||
chr2:207577349 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-156G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207577349 | |||||||
chr2:207577371 | G | A | 32 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(29): Show |
34 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.689-134G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 6/7 | chr2 | 207577371 | |||||||
chr2:207577929 | C | T | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.839+274C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207577929 | |||||||
chr2:207578147 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.839+492A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578147 | |||||||
chr2:207578287 | G | A | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+632G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578287 | |||||||
chr2:207578648 | T | A | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+993T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578648 | |||||||
chr2:207578785 | C | CAAGTG | 3 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 |
3 | HG02145.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.839+1132_839+1136d others(7): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207578785 | ||||||
chr2:207578847 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.839+1192A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578847 | |||||||
chr2:207578862 | C | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0140 a0001c0001t0003g0141 others(9): Show |
13 | HG00140.hp1 HG00323.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.839+1207C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578862 | |||||||
chr2:207578909 | A | G | 1 | a0001c0001t0059g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.839+1254A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578909 | |||||||
chr2:207578988 | A | G | 4 | a0001c0001t0015g0255 a0001c0001t0015g0256 a0001c0001t0015g0257 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+1333A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207578988 | |||||||
chr2:207579098 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.839+1443T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207579098 | |||||||
chr2:207579241 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.839+1586A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207579241 | |||||||
chr2:207579285 | G | GATCAAGA others(1): Show |
4 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+1631_839+1638d others(10): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207579285 | ||||||
chr2:207579304 | C | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(125): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.839+1649C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207579304 | |||||||
chr2:207579601 | C | G | 4 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+1946C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207579601 | |||||||
chr2:207579691 | T | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(256): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.839+2036T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207579691 | |||||||
chr2:207579894 | C | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.839+2239C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207579894 | |||||||
chr2:207580136 | A | G | 1 | a0001c0001t0003g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.839+2481A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580136 | |||||||
chr2:207580168 | A | G | 1 | a0001c0001t0004g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.839+2513A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580168 | |||||||
chr2:207580273 | T | C | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.839+2618T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580273 | |||||||
chr2:207580348 | A | G | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.839+2693A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580348 | |||||||
chr2:207580429 | T | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(280): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.839+2774T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580429 | |||||||
chr2:207580729 | A | G | 1 | a0001c0001t0008g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.839+3074A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580729 | |||||||
chr2:207580952 | A | G | 2 | a0001c0001t0003g0123 a0001c0001t0003g0127 |
2 | HG02273.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.839+3297A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207580952 | |||||||
chr2:207581053 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.839+3398C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581053 | |||||||
chr2:207581245 | C | T | 1 | a0001c0001t0007g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.839+3590C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581245 | |||||||
chr2:207581339 | T | C | 1 | a0001c0001t0006g0263 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.839+3684T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581339 | |||||||
chr2:207581418 | CAA | C | 3 | a0001c0001t0023g0023 a0001c0001t0023g0259 a0001c0001t0023g0260 |
3 | HG02818.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.839+3765_839+3766d others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207581418 | ||||||
chr2:207581480 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.839+3825C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581480 | |||||||
chr2:207581643 | T | G | 260 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(257): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.839+3988T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581643 | |||||||
chr2:207581704 | A | G | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.839+4049A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581704 | |||||||
chr2:207581811 | C | G | 1 | a0001c0001t0004g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.839+4156C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207581811 | |||||||
chr2:207582030 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.839+4375G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582030 | |||||||
chr2:207582095 | T | G | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.839+4440T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582095 | |||||||
chr2:207582521 | A | G | 1 | a0001c0001t0029g0213 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.839+4866A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582521 | |||||||
chr2:207582534 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.839+4879A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582534 | |||||||
chr2:207582560 | A | G | 8 | a0001c0001t0003g0006 a0001c0001t0003g0141 a0001c0001t0003g0145 others(5): Show |
9 | HG00140.hp1 HG01099.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.839+4905A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582560 | |||||||
chr2:207582745 | T | G | 1 | a0001c0001t0002g0236 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.839+5090T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582745 | |||||||
chr2:207582751 | G | A | 2 | a0001c0001t0005g0031 a0001c0001t0005g0262 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.839+5096G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582751 | |||||||
chr2:207582790 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.839+5135G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582790 | |||||||
chr2:207582894 | AAAAC | A | 64 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(61): Show |
67 | HG00642.hp1 HG01109.hp2 HG02027.hp1 others(64): Show |
intron_variant | MODIFIER | c.839+5255_839+5258d others(6): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207582894 | ||||||
chr2:207582910 | C | A | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+5255C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582910 | |||||||
chr2:207582914 | A | C | 4 | a0001c0001t0011g0027 a0001c0001t0011g0191 a0001c0001t0025g0007 others(1): Show |
5 | HG01168.hp2 HG01169.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+5259A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582914 | |||||||
chr2:207582916 | A | AT | 22 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(19): Show |
23 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.839+5261_839+5262i others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582916 | |||||||
chr2:207582916 | A | T | 1 | a0001c0001t0006g0263 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.839+5261A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582916 | |||||||
chr2:207582918 | A | T | 243 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(240): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.839+5263A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582918 | |||||||
chr2:207582930 | T | C | 1 | a0001c0001t0016g0012 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.839+5275T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207582930 | |||||||
chr2:207583333 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.839+5678G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207583333 | |||||||
chr2:207583336 | G | A | 1 | a0001c0001t0010g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.839+5681G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207583336 | |||||||
chr2:207583390 | T | G | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.839+5735T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207583390 | |||||||
chr2:207583823 | T | C | 17 | a0001c0001t0004g0292 a0001c0001t0010g0026 a0001c0001t0010g0183 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.839+6168T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207583823 | |||||||
chr2:207584023 | C | G | 5 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(2): Show |
5 | HG01884.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.839+6368C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584023 | |||||||
chr2:207584131 | G | A | 1 | a0001c0001t0003g0293 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.839+6476G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584131 | |||||||
chr2:207584260 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.839+6605T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584260 | |||||||
chr2:207584271 | A | G | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+6616A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584271 | |||||||
chr2:207584422 | G | A | 18 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(15): Show |
19 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.839+6767G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584422 | |||||||
chr2:207584511 | C | G | 1 | a0001c0001t0015g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.839+6856C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584511 | |||||||
chr2:207584670 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.839+7015G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584670 | |||||||
chr2:207584686 | G | A | 2 | a0001c0001t0003g0045 a0001c0001t0003g0046 |
2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.839+7031G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584686 | |||||||
chr2:207584882 | A | T | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.839+7227A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207584882 | |||||||
chr2:207585061 | G | C | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.839+7406G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207585061 | |||||||
chr2:207585127 | G | A | 1 | a0001c0001t0040g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.839+7472G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207585127 | |||||||
chr2:207585224 | G | T | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.839+7569G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207585224 | |||||||
chr2:207585989 | G | A | 4 | a0001c0001t0015g0255 a0001c0001t0015g0256 a0001c0001t0015g0257 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+8334G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207585989 | |||||||
chr2:207586042 | A | G | 1 | a0001c0001t0010g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.839+8387A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586042 | |||||||
chr2:207586051 | T | C | 1 | a0001c0001t0035g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.839+8396T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586051 | |||||||
chr2:207586064 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(116): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.839+8409C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586064 | |||||||
chr2:207586442 | G | C | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+8787G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586442 | |||||||
chr2:207586496 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.839+8841T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586496 | |||||||
chr2:207586514 | T | A | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.839+8859T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586514 | |||||||
chr2:207586638 | A | G | 1 | a0001c0001t0004g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.839+8983A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586638 | |||||||
chr2:207586699 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.839+9044G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586699 | |||||||
chr2:207586777 | A | G | 1 | a0001c0001t0037g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.839+9122A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207586777 | |||||||
chr2:207587029 | G | T | 1 | a0001c0001t0004g0105 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.839+9374G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207587029 | |||||||
chr2:207587235 | T | C | 3 | a0001c0001t0023g0023 a0001c0001t0023g0259 a0001c0001t0023g0260 |
3 | HG02818.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.839+9580T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207587235 | |||||||
chr2:207587320 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(285): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.840-9594A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207587320 | |||||||
chr2:207587369 | G | A | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.840-9545G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207587369 | |||||||
chr2:207587379 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.840-9535C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207587379 | |||||||
chr2:207588020 | A | G | 1 | a0001c0001t0002g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.840-8894A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588020 | |||||||
chr2:207588074 | T | C | 1 | a0001c0001t0024g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.840-8840T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588074 | |||||||
chr2:207588139 | C | CTTT | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(280): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.840-8775_840-8774i others(5): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588139 | |||||||
chr2:207588191 | A | G | 4 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(1): Show |
5 | HG03195.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.840-8723A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588191 | |||||||
chr2:207588353 | T | G | 2 | a0001c0001t0054g0294 a0001c0001t0059g0295 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.840-8561T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588353 | |||||||
chr2:207588387 | G | C | 1 | a0001c0001t0004g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.840-8527G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588387 | |||||||
chr2:207588399 | T | C | 2 | a0001c0001t0031g0122 a0001c0001t0032g0119 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.840-8515T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588399 | |||||||
chr2:207588728 | GT | G | 156 | a0001c0001t0001g0039 a0001c0001t0001g0089 a0001c0001t0001g0147 others(153): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.840-8172delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207588728 | ||||||
chr2:207588728 | GTT | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(79): Show |
83 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.840-8173_840-8172d others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207588728 | ||||||
chr2:207588737 | T | TG | 5 | a0001c0001t0005g0276 a0001c0001t0005g0284 a0001c0001t0006g0280 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.840-8177_840-8176i others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588737 | |||||||
chr2:207588739 | T | G | 21 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0219 others(18): Show |
22 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.840-8175T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588739 | |||||||
chr2:207588739 | T | TG | 23 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(20): Show |
24 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.840-8175_840-8174i others(3): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588739 | |||||||
chr2:207588741 | T | G | 153 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0039 others(150): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.840-8173T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207588741 | |||||||
chr2:207588889 | C | CG | 32 | a0001c0001t0004g0065 a0001c0001t0005g0031 a0001c0001t0005g0262 others(29): Show |
33 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.840-8017dupG | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207588889 | ||||||
chr2:207589427 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(256): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.840-7487A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207589427 | |||||||
chr2:207589534 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.840-7380C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207589534 | |||||||
chr2:207589698 | A | G | 2 | a0001c0001t0003g0154 a0001c0001t0003g0161 |
2 | HG02015.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.840-7216A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207589698 | |||||||
chr2:207589830 | T | C | 1 | a0001c0001t0007g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.840-7084T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207589830 | |||||||
chr2:207589915 | C | T | 28 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(25): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.840-6999C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207589915 | |||||||
chr2:207590082 | AGTTTT | A | 26 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(23): Show |
27 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.840-6831_840-6827d others(7): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207590082 | |||||||
chr2:207590083 | G | GT | 164 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(161): Show |
172 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.840-6807dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207590083 | ||||||
chr2:207590083 | G | GTT | 20 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0061 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.840-6808_840-6807d others(4): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207590083 | ||||||
chr2:207590083 | G | GTTTT | 7 | a0001c0001t0012g0009 a0001c0001t0012g0042 a0001c0001t0012g0043 others(4): Show |
7 | HG02886.hp1 HG03195.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.840-6810_840-6807d others(6): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207590083 | ||||||
chr2:207590107 | T | A | 3 | a0001c0001t0003g0131 a0001c0001t0018g0115 a0001c0001t0049g0152 |
3 | HG00323.hp2 HG02897.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.840-6807T>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207590107 | |||||||
chr2:207590107 | T | TA | 52 | a0001c0001t0001g0039 a0001c0001t0001g0147 a0001c0001t0003g0006 others(49): Show |
54 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.840-6805dupA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207590107 | ||||||
chr2:207590111 | A | T | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.840-6803A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207590111 | |||||||
chr2:207590112 | G | A | 1 | a0001c0001t0060g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.840-6802G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207590112 | |||||||
chr2:207590356 | T | C | 2 | a0001c0001t0028g0073 a0001c0001t0028g0172 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.840-6558T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207590356 | |||||||
chr2:207590447 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.840-6467G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207590447 | |||||||
chr2:207591555 | C | A | 8 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(5): Show |
9 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-5359C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207591555 | |||||||
chr2:207591581 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0028 a0001c0001t0002g0030 others(60): Show |
66 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(63): Show |
intron_variant | MODIFIER | c.840-5333C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207591581 | |||||||
chr2:207591675 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18944.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.840-5239C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207591675 | |||||||
chr2:207591676 | G | A | 1 | a0001c0001t0023g0023 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.840-5238G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207591676 | |||||||
chr2:207591984 | T | C | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.840-4930T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207591984 | |||||||
chr2:207592249 | T | C | 3 | a0001c0001t0003g0296 a0001c0001t0054g0294 a0001c0001t0059g0295 |
3 | HG02145.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.840-4665T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592249 | |||||||
chr2:207592279 | C | T | 1 | a0001c0001t0035g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.840-4635C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592279 | |||||||
chr2:207592280 | G | A | 1 | a0001c0001t0004g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.840-4634G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592280 | |||||||
chr2:207592332 | G | A | 1 | a0001c0001t0005g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.840-4582G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592332 | |||||||
chr2:207592339 | A | G | 266 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(263): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.840-4575A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592339 | |||||||
chr2:207592638 | T | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(263): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.840-4276T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592638 | |||||||
chr2:207592896 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.840-4018A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207592896 | |||||||
chr2:207592911 | C | CAAAAAAG others(14): Show |
263 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(260): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.840-3992_840-3991i others(23): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207592911 | ||||||
chr2:207592911 | C | CAAAAAAG others(14): Show |
1 | a0001c0001t0018g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.840-3987_840-3986i others(23): Show |
CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207592911 | ||||||
chr2:207593018 | C | T | 15 | a0001c0001t0002g0209 a0001c0001t0002g0224 a0001c0001t0007g0003 others(12): Show |
17 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.840-3896C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593018 | |||||||
chr2:207593113 | A | G | 7 | a0001c0001t0010g0026 a0001c0001t0010g0183 a0001c0001t0010g0184 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.840-3801A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593113 | |||||||
chr2:207593185 | T | G | 1 | a0001c0001t0050g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.840-3729T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593185 | |||||||
chr2:207593194 | A | G | 266 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(263): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.840-3720A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593194 | |||||||
chr2:207593254 | G | A | 129 | a0001c0001t0001g0039 a0001c0001t0001g0147 a0001c0001t0002g0002 others(126): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.840-3660G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593254 | |||||||
chr2:207593405 | C | T | 18 | a0001c0001t0005g0031 a0001c0001t0005g0262 a0001c0001t0005g0272 others(15): Show |
19 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.840-3509C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593405 | |||||||
chr2:207593407 | A | G | 1 | a0001c0001t0003g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-3507A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593407 | |||||||
chr2:207593719 | CT | C | 248 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(245): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.840-3175delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207593719 | ||||||
chr2:207593750 | C | T | 1 | a0001c0001t0005g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.840-3164C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593750 | |||||||
chr2:207593755 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.840-3159A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593755 | |||||||
chr2:207593884 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.840-3030A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593884 | |||||||
chr2:207593938 | C | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0236 |
2 | NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.840-2976C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207593938 | |||||||
chr2:207594817 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.840-2097A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207594817 | |||||||
chr2:207594991 | C | CT | 14 | a0001c0001t0001g0020 a0001c0001t0001g0061 a0001c0001t0001g0174 others(11): Show |
14 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.840-1902dupT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207594991 | ||||||
chr2:207594991 | CT | C | 12 | a0001c0001t0001g0088 a0001c0001t0001g0203 a0001c0001t0003g0143 others(9): Show |
12 | HG01070.hp2 HG01099.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.840-1902delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207594991 | ||||||
chr2:207595002 | T | C | 1 | a0001c0001t0002g0290 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.840-1912T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595002 | |||||||
chr2:207595098 | T | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(263): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.840-1816T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595098 | |||||||
chr2:207595137 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.840-1777A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595137 | |||||||
chr2:207595419 | AT | A | 5 | a0001c0001t0003g0131 a0001c0001t0003g0133 a0001c0001t0003g0148 others(2): Show |
6 | HG00140.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.840-1485delT | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207595419 | ||||||
chr2:207595502 | C | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0030 a0001c0001t0002g0160 others(2): Show |
7 | NA18952.hp1 NA18962.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.840-1412C>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595502 | |||||||
chr2:207595571 | A | C | 1 | a0001c0001t0010g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.840-1343A>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595571 | |||||||
chr2:207595644 | A | G | 2 | a0001c0001t0011g0027 a0001c0001t0011g0191 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.840-1270A>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595644 | |||||||
chr2:207595724 | T | G | 1 | a0001c0001t0051g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.840-1190T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595724 | |||||||
chr2:207595742 | A | T | 2 | a0001c0001t0007g0244 a0001c0001t0007g0245 |
2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.840-1172A>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595742 | |||||||
chr2:207595823 | C | T | 4 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-1091C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595823 | |||||||
chr2:207595849 | G | A | 1 | a0001c0001t0010g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.840-1065G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595849 | |||||||
chr2:207595870 | T | G | 1 | a0001c0001t0041g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.840-1044T>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595870 | |||||||
chr2:207595957 | C | T | 1 | a0001c0001t0024g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.840-957C>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595957 | |||||||
chr2:207595963 | G | C | 1 | a0001c0001t0004g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.840-951G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207595963 | |||||||
chr2:207596028 | G | A | 4 | a0001c0001t0022g0197 a0001c0001t0022g0198 a0001c0001t0022g0199 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-886G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596028 | |||||||
chr2:207596179 | G | A | 1 | a0001c0001t0022g0198 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.840-735G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596179 | |||||||
chr2:207596325 | G | C | 1 | a0001c0001t0011g0191 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.840-589G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596325 | |||||||
chr2:207596410 | G | T | 2 | a0001c0001t0054g0294 a0001c0001t0059g0295 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.840-504G>T | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596410 | |||||||
chr2:207596439 | G | C | 1 | a0001c0001t0003g0149 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.840-475G>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596439 | |||||||
chr2:207596476 | C | G | 1 | a0001c0001t0003g0040 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.840-438C>G | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596476 | |||||||
chr2:207596665 | T | C | 3 | a0001c0001t0023g0023 a0001c0001t0023g0259 a0001c0001t0023g0260 |
3 | HG02818.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.840-249T>C | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596665 | |||||||
chr2:207596692 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0003g0040 |
2 | NA18946.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.840-222G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596692 | |||||||
chr2:207596710 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.840-204G>A | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | chr2 | 207596710 | |||||||
chr2:207596839 | GA | G | 12 | a0001c0001t0010g0026 a0001c0001t0010g0183 a0001c0001t0010g0184 others(9): Show |
12 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.840-65delA | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207596839 | ||||||
chr2:207596897 | TC | T | 8 | a0001c0001t0001g0168 a0001c0001t0004g0025 a0001c0001t0004g0167 others(5): Show |
9 | HG00099.hp1 HG01081.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.840-15delC | CREB1 | ENSG00000118260.15 | transcript | ENST00000353267.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 207596897 |