Tag | Content |
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EnhancerAtlas ID | HS059-01135 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:33077590-33078680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr1:33078054-33078071 | CAGCTCACTGTGACCTC | - | 6.48 | ZNF263 | MA0528.1 | chr1:33078396-33078417 | GGAGAAGAGAAAGGAGAGGGA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 33077721 | 33078012 | chr1 | 33077800 | 33078400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I032611 | chr1 | 33077361 | 33078639 |
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Enhancer Sequence | CGTCCTCATT TAAAACAGTT GGACTTGGGG GGTTGTGCAC TGGAATGACT AACCTGGAAG 60 CCACGCCACG ACTCAGGGGC GGAGGGGACT CGAATCCGCG CGATCAGATG CCGCCGCAGG 120 TGCTTAAGAC CTGCAGCCTA CAGAGCAAGC CTATCTTATC CCCACTTTAG GAAAAGTTGT 180 CTGGTGTTAC TTAAGGTTAT GACATTGTGC TCTGTGAAGT CACTTGCGTC CCCGACACCT 240 CCCAACTCAG CTGGGACTGG CCAGTGCCCT GCTCCCTGAC CTCGCCGCGG CGGCCAGTAG 300 GAGGTGTCGG CGCCCCAGGA GTCCGCGGCC GAGCCAATGG GAGCCGCGAG AAGGGCCGGG 360 GCGGAGCCTG GACGCGTGAT GCCAGGGAAC CACTCCCGTG GGATTTGGCC AGAGGCATCT 420 CACTGGCGTC CTGTCGCCCA GGCTGGGGTG CAGTGGCTCG ATCTCAGCTC ACTGTGACCT 480 CTGCCTCCCG GGTTGAAGCG ATTCTTCCGC CTCAGCCTCC CTAGTATCTG AGATTATGGG 540 CGTGCGCCAC ATGCCCGGCT AATTTTTTTG TATTTTTATT AGAGACGAGG TTTCACCATG 600 TTGGCCAGAC TGGTCTTGAA CTCCTGGCCT CATGTGATCC ACCCACCTCG CCTCCCAAAG 660 TGCTGGGATT ACAAGCGTGA GCCACCGCGC CTGGCCTGAA GTGCAGGCTT TTGAATATAG 720 ATGCTCAACG AAGATATGGG AGAAAGAAAG CTAGATTAGC ACAGGAAAAA GCCACAGTAG 780 ATAAGTAGGA GACGGGAAAT AAGTCTGGAG AAGAGAAAGG AGAGGGAAAA GCAGAAACGA 840 GTGACTCAGC CTGCCCAGCT TAATAAACTA AGATTCTAGC TACCATGTCA CTTGTGCAGA 900 TGGCACGGGC TCCCAGGGTT GTCTCTAGAA TGATGACACC CCTTCACCAA GCACTGTGGA 960 CCTTCTTTAG AATTAAAGAG GGGGCTGGAC ACAGTGACTG ACGCCTGTAA TACCAGCACT 1020 TTGGGAGGAG GAAGTGGAAG GATTGCTTGA GGCCAGGAGT TTGAGACCAG CCTGGGCAAA 1080 ATACTGCCTT 1090
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