| Tag | Content |
|---|
EnhancerAtlas ID | HS080-08551 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr12:81603210-81604450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr12:81603804-81603821 | AAGGTCTTTGTGACCTG | - | 6.09 | | ESR2 | MA0258.2 | chr12:81603805-81603820 | AGGTCTTTGTGACCT | - | 6.63 | | Pou2f3 | MA0627.1 | chr12:81603696-81603712 | TATAATTAGCATATAA | - | 6.49 | | SREBF2 | MA0596.1 | chr12:81604046-81604056 | ATGGGGTGAT | + | 6.02 | | SRF | MA0083.3 | chr12:81603609-81603625 | AGACCATATAGGGTAA | - | 6.07 | | STAT3 | MA0144.2 | chr12:81603578-81603589 | CTTCCCAGAAG | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I081209 | chr12 | 81603537 | 81604141 |
|
Enhancer Sequence | CAACAACCAT ATCTCATGAT TTTGTGGATC ATAGGCAGAA ATCAGCCAGG GATTCTGGTG 60
CTCCAAGTCT CCAAGTATTG TTGACTAAAA CAACCCGGAC AGTATTCAGT GATGAATTTG 120
TTACCTGAAA GAGCTCCTGA TCCAGACCGC AAGAAGGGGT TCTTGGACCT CACACAAGAT 180
TGAATTCAGG GCAAGTCCAT AGAGTAAAGT GAAAGCAAGT TTATTAGGAA AGTAAAGGAA 240
AAAAAGAGTG CTACTCCATA GGAAGAGCAG CCCGAACGGC TACTGGTTGG CTATTTTTAT 300
GGTTATTTTT AATTATATGC TAGACAAGGG GTGGATGTTT TATGAGTTTT CCAGAAAAGG 360
GGTGAGCACT TCCCAGAAGT GCGGGTCCCT CCCCTTTTTA GACCATATAG GGTAACTTCC 420
TGACATTGCC ATGGCATTTG TAAACTCATG GCACTGGTGA GAGTGTCTTT TAGCATGCTA 480
ATGCATTATA ATTAGCATAT AATGAGCAGT GAGGATGACC AGAGGTCAAT TTCATGACCA 540
TCTTTGTTTT GGTGAGTTTT GGCCAGCTGC TTTACCTCTT GCTGTTTTAT CAGCAAGGTC 600
TTTGTGACCT GTATCTTGTG CCAACTTCCT GTCTCATCCT GTGACTAAGA ATGCCTAACC 660
ACTTTGGAAA GCAGCCCAGT AGGTCTCAGT ATTATTTTAC TCAGCCCCTA TTCAAGATGG 720
AGTTGCTCTG GTTTGAATGC CTCTGACATA TTTTCCCCTT CCCTTTTATA AGAGAAACCT 780
AATCCTAAGG GTCGTAGACA GATTAAAATC CATCTTCTGT AACTTCTTCA GGCTGAATGG 840
GGTGATGATA TTCCTGCCTA TTAGGGTCTC TCGTATTCAG GTTAGAGAGG AGCTTCGTCA 900
GAAAGCATCA GTATGTTGAG GACCACTCAT AACTCTTGGA TTCCATCAAA AGGTGATATC 960
TGAAAGATTT AAACGTGTTC AATTTAAGAG GACATTGAGA AAGCTTATCC TGCATTCCTA 1020
CACATAGAGT ACAACAGCAA TATATTCCAC AATAGTATAG CAAAATAAGT AAAAACTATC 1080
CCAAGTAAAC TAAATAAGAA GGCTATGAAC CTGGCAACTG TTGGAACCAA ACTGATATGG 1140
GGATGCTAGC TGATTCCAAT ATATACCCAG AATTAGAATA CTAATCTGGA ATTTTACATT 1200
ACCCATCTCT TTTGTTTCTT CTGAGCTGCA GTCAGAGATC 1240
|
