Tag | Content |
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EnhancerAtlas ID | HS136-04793 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr12:76357500-76358990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr12:76357985-76357998 | TTCTAGAAAATTC | + | 6.34 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_43644 | chr12:76356896-76360417 | MM1S | SE_47123 | chr12:76350711-76361195 | Panc1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I075963 | chr12 | 76356897 | 76360417 |
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Enhancer Sequence | ATCATGTTAT TTCTCATAAC AACCCTGTAA ACTGAGTATT ATTTTTCCAA TTTTTCAAAT 60 AAGAAAACTA AGACTCAGAG AACTTGGGTA ACCTGCCCAA GGCCATAAGT CTCAAATATA 120 GAAGCTCTGG AATTTCAAAC AGGTTAGTTC ATTCATTCAT ATATCCATTG ATTCATTCCC 180 TCAACATTCA AAATAGTTAT TGAGTATATT CCCTGTGCCA GGAACCAGTG AAGCTAGGTT 240 TTGGTTATCA ACAAACAAGA TGGATGCTAT TCCTGTCTTA GAGGGATTTA TCTTCAGTCT 300 GATTCCAAAT CCTGTTTCTT TACCACTACA TGTATCATTT CCCAAATTAG GGATCAAACA 360 GTCATACCAG TTAGTATAGT ATACCTTAAC CTGGAAAAGA ACTGACACCT TCACTTACAT 420 GGAGACTGTA GCCTGATATA CCCTGCCATC ACCCTTCACA AGCAAAAGGA AAAATTTCTA 480 AAGAGTTCTA GAAAATTCAG ACTATATTCT GGAAGTACAA CTCTAGAAGC CTGGGACCTC 540 TGCATTCTAG TTCTGCTCAG TTTGAATATG GCACTAATGT GGAAGTCCAC GAGTGTCTGT 600 CACTCATGGC TGGCCACACC CCCTATTCTT GCACAGGTTC CCTCCCTGCC TGAGGAAGTA 660 TTTCTAACAG ATATTTCAGT TCACTTCCTT CTCAGGCTGG CCTTGCCTCA CTTCTAGGAT 720 TGTTTCTCTA TCCATCTCCT ACACACAGCC AGGCCACACA GGTAGGTTCC TACTTAGTAT 780 TTTAGTATGA TTTCAGAAAT ACTGAGAAGC TAACAGTACC ATCTCCTTCT CCAGGGCTAC 840 TGCACTGCCC ATCTGCAGGG GCACAGACAA CAGGATATGA TAGGTGCCCC TGGGAGAAGA 900 GGCTCTGTCT CTCCTCTCCC ACAACACACT ATTAATTCCT TACATACTCC CAAATGCCCC 960 CAAATATACC AACATTTCCT TCTGCATTTA GAAAATTTTA AATGCAAATG ACCTTCTAAA 1020 AGATCATATT CGGCAGACAG CGACAGACGG AGCTGCGGAC CAAATTGGAA CCTCTGGCTT 1080 AAGAGTAATC ATGTTTCTTC AGTATTAGTG AGCAGGGAGA TCAGGTCTAT ACGCTGGAGA 1140 AATTTGACTC GATGGGACAA CAGACCTGCT TAGCCCATCC TGCTCAGTTC TCCCCAGATG 1200 ACAAATATTC CCGACACCGA ATCACCATCA AGAAACGTTT AAAGGTGCTC ATGACCCAGC 1260 AACCGCGCCC TGTCCTCTGA AGGTCCCTTA AACTGATGTC TCTTCTGCCA CCTGTTACCC 1320 CCTAGAGACT CCGTAACCAA ACTCTTCAAT CTGTGAGCCC TGATGCCTTT TTGCCAGCCA 1380 TGCTCTTTGG CATCCAGTCT CATCATGGTG ATTGATCATG CTTGTGCGAG GCAATCATGG 1440 TGGCATCACC TGTAAAGGGA ACACGTTTAA CTTTTTTTCT CATATTTTAA 1490
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