Tag | Content |
---|
EnhancerAtlas ID | HS007-15147 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr7:2872380-2873870 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr7:2873355-2873366 | AGGCCATAAAA | + | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65520 | chr7:2871754-2872897 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 2873337 | 2873533 | chr7 | 2873637 | 2873687 | chr7 | 2873752 | 2873835 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I002830 | chr7 | 2870119 | 2873300 |
|
Enhancer Sequence | TCTACTTGGT CTCTACTTAA GAAAGTGGGG GTCAGGGATG TTTTCTTCCC CTTGCCGTCC 60 AGAGCGGCTG GATGTGCTGC CCTCCAGCAC CTTTCTAGCT GCTTGCAAGA GCTCCCACCC 120 TCTGCTTCTC TGTCCTCTGG ATGCCGCACT TCCAAAGCAG ACGTTCCAAA TGCATTTGGT 180 CAACAGAATC AACCAGAAGC ATGAGCTTCT CTAACGGCTA ACACAGGATA CAAGTCATGT 240 TTTCCATTCT GCAAAACCTG GACACACCTG AGCATTTATC CTCACAGAGA GAAAGACTAA 300 CCCATCACAC GGTCAGCAAC AAATATTCAC ATTCGGCTTT TAGGATTAAA AGGCAATCCG 360 GTGGTCCTGA GCAGCTGCTC TGTCCAGCCC ACTTGAAGCC TCCATTTCTT TTAAGTACAA 420 ACAAACCATA ATAGTTACGG CATGAAATGA GCCGGCCTGT CATCATGGGA TGGCACTGCC 480 CTTCAGGTGA TGCAAGTTAA GCCCTAGGTC CATTACACAA CATCAGCTTC TTTGGTTTGA 540 ACATCACCCT ATAATTACAT CTCTAGATAA GGCCGAAGTT TAAATCTTCA GTTCCATTTA 600 AAACCGGTAC GATCCATGAA CCCACTCTCA ACTGAGTAAG AACAGAAAAT AATTACGAGC 660 TGTCAACGGA ACACTATCTC ACATCAAGCA CAGCTGGCTT CCAAATCTCA CATGACAGAT 720 GACTGAAGGT CAAACCCTGC TCCCCCTAAT TATTTCGTTA AGATAATCAA CATGTAAACT 780 CGAAAGCCAG GGGACAAGAC CAATCACTCA TGTGTTCTGA ATCCCCAAAA ATGGCCAGAG 840 GAGTCTCTCT GGACTTAGTT AGCTGACGGA AAAAGATGTT TTTGCATTTG TTTTGTTTGG 900 TTTTTTGGTA TTACGAAAGG ACCAACCCCG TATGTCAAAG CATAAGGTAA ACCTGTTAAA 960 TGCAATTTGC CAACAAGGCC ATAAAAACCA AACTGTGCTT CCAGACCCCA GAAGCAGATG 1020 TATGCTTCTG CCGCCACGCA AACCCGCCGC AGCATCAAGC CTAAAGAGGC ACTTCTGAAC 1080 TCCCAAGACA GAGACTCTTA AAGGCCAGAA CAGCAGAGGA GGCTGCTTCA AAGTTCCGTA 1140 CGTCCTGGCA AAAAGTACAT GTGATACAGC AAACAATTCT TCAAAAAAAA AATTTAATTT 1200 CCAAAATTTT TACATAATCT TTGATATTCC ACAACAAAAG CTGTTAACCT GCAGTGCATG 1260 GGCCACTAGT AGGCCCACTC TTGGGATTCC GGATGTCCAA ACACTCCCCT GAAACCCTAC 1320 ACAGATACAT GAATTTTCTA GGGAGAAGAC CCACAGCTTT CAGCTAGAGT GCTGCGACTG 1380 CAGTCCAAAG AAAGCCACCA CATTACAACC ACTCCTTTGG ACTAGAAAGT TCTGATTCTT 1440 TAGTATCTCT ATGTATTCGA ATTTTCTGTC TTAGCTGATA AATGTAGAGG 1490
|