| Tag | Content |
|---|
EnhancerAtlas ID | HS007-11375 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:72377890-72379070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr3:72378764-72378774 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr3:72378764-72378774 | GTCACGTGAC | - | 6.02 | | MEF2A | MA0052.3 | chr3:72378781-72378793 | GCTATTTTTAGC | - | 6.44 | | MEF2B | MA0660.1 | chr3:72378781-72378793 | GCTATTTTTAGC | - | 6.92 | | MEF2C | MA0497.1 | chr3:72378780-72378795 | AGCTATTTTTAGCCT | - | 6.92 | | ZNF263 | MA0528.1 | chr3:72378855-72378876 | GGGGGATGGGGAGGGAAAGAA | + | 6.31 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 72378494 | 72378958 | | chr3 | 72378543 | 72378800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I072329 | chr3 | 72378701 | 72378850 |
|
Enhancer Sequence | GTTTAGGGTT GCTGCAAGCA GCGATAAGAG AGGGAAGAGA AGAGAAAAAA GGGGCTAGGG 60
AAAAAGAAGA AAGGGGCGGG GGTCACAGCA CCTAGGATGG CAGTTTTCAA AGGTTGCTCC 120
TGGAGCACAG CATCTAGGAT GGCAGTTCTC AAAGGTTGCT CCTGGAGCAC AGCATCAGCA 180
TCACACAAGG ACTTGCTGGA AATGCAGATT CTTGAGCCCA GCCCCAGACC TGCTGGAGGA 240
GAAATTCCAG GGCCAGCGTC CAGCATCCAG TGTGTTAAGA AGCCCTCCGC GTTACTGTAA 300
TGCCCTCAAG TTTGGGTCTC TTGGGACTGG TCCAGGGTGC TGGAAGTTAT TCTATATTCG 360
GAGGAGGAAC TTGGGAGGAG TCCAGAAAGG CTTCCTTGGG GGATATTTGT CAACAGATTT 420
ACCTTTACTC CCAAATAATA AAATAGCTTT AGTTGCAAGG AGTTGGTGAG GGAACCAAGT 480
GGGCAGGGAG CATGGGTACC TGAGAGAAAA ACCCATCTCT CTTGCTGGCA AAGACATGCC 540
TTGCCTGCTC GCTGGGAAAG GGATGGGGAC ACGGTGTCCA GGTATGAGAA AGCCCTTGCC 600
TCCAAGACCG TTGCTCCTGA AGGGAAGGGG CAGCTTCTGG CTCTGAGCCC GGAGCACCAG 660
GCCTGGGGTC TGCCAGTTCT GAGGGTGCTA TTGCCCTCTC TGCCCCCCCG CCCTCCGTCT 720
GTCACACTGG AGGATGTCAC AGGAAACAAT GTGCCCCTGC GAGGGCCCGG CTGCATTGGC 780
AGCGGCCTGG CTTCAGGCAT CACAATGACT CTCATTTCCT AGGAAACAGG GAGTCGCACT 840
TGCACCTTTG CTGGGAGCCT CCGCATTTGG AGCTGTCACG TGACTCGGGG AGCTATTTTT 900
AGCCTCCCCA GCCCTGTGTT GTAGGAAGAA TGATTTGATG AAAATACTAA ACTCATTAAA 960
AGCCTGGGGG ATGGGGAGGG AAAGAAGGGC TGCCAGAGTG GGGAGGCTAC AGCCTCCAAG 1020
ATTCCAACCC AGGCTGAGCA GCACAGAGGT AAAGACAGCA GGGACCTGGT ATTTCCACGG 1080
GCACCGTGCC CTGGGGAGCT GGGGCAGTAG GGACTATTAA CTCTAATACC CGGTACTGCT 1140
GGTCAGTACT ATGGGCCAAG CGCTATGCAC AATACTTTAC 1180
|
