Tag | Content |
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EnhancerAtlas ID | HS098-35352 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr20:61896900-61898050 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr20:61897463-61897476 | TTCTAGAATTTTC | + | 6.71 |
| | 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 |
GH20I063264 | chr20 | 61895831 | 61901241 |
| Enhancer Sequence | GAAGCTGGTA ATGCCCACCA CTCGGTCACC AGTGTTGGTA CCGCTCTGGC TGTCGGCAAC 60 TGGCTGGGCC TGGGGACACA TGGGAACAAC TCCGATCACA CAGGAAGAGT TTCCCGGTCC 120 CTCGGGACCA TGGAAGCCCA GCCACACAGC ACCGGTTTGA GGCAAGGCTC TCAATACCTC 180 GCCCTCCGTG CCCAACACCT TGGTCTTCTG CTAGGGGTCC TCACAGTCTG GGGAAACTGA 240 GTCCACATGG GCCTCAGGGC TGGAGCTTGG AGCCCAGGGC ACCCAGTCAG CACATTCTAT 300 CCTCCTGGCC GGTGATTGTT TGGAAGTGGA CACATGACCC CAGCTAGGCC CATCAGGGTG 360 GAGCGTGAGC TTTCAGCTGG GATGCCGGTG CAAGGCTACT TTCTCTTGCT GGAGGCGAAT 420 CATGAAGCTT GCAGCCTTAG AAGCTGCCAG AAGCATCCTG GGGTCTCAGG ATGAAGACGG 480 AACTGCAAAC ATACACAGAG AATCCTGGTT CTCAGCAATA GTGCTGAGCT GCTGGATCAA 540 GCCACACCTG AAATTGAACT TTGTTCTAGA ATTTTCATCA CACAAATCAA TACATTCCCT 600 TTGCTAAGCC ATTTGGGGTT GAGATTTTTG CCTCTAGCAA CTAGAATCTG GAAAGATTCC 660 TGGCTAAGAT ACGCATGGGA GGGTCCAAAG CAGGAGGACC CTGCGGGTCC AGCTGTCACA 720 GCCCCAGGAT CTGAGCTACC AGTTCTGCAA TCTGAGAAGC TGGCCTGGTC TCAGCACATT 780 CTTAGCTGTG ACTCCTTAGC CGCTGTGGCC ACACGTAATT CAGCACAGCT GCAAGTTTCT 840 TGGAGCTCAG GACAGAGCGG CTCAGCATTT TCGAGGAACA TTTGTACTTC TGGGTGACTT 900 ACACACCCTG ACATTCTTCC CATTTCCTTC TGTCCTGGGC CCCAGTTCTT CTGGACGCCA 960 CGCACAGGCA GCAGAAGTGG GGGCAGACGG GGCTGGAACC AGCCAGGTGG AGTCCCACCA 1020 TGCAGCAGGC CAGAAGCCAG GACCAAGGCA GCACCGTCGT GGGCAGCCCC GGGCCAACCC 1080 CACGCGCTTC TCTCCAGGAC CCAGGCGGCA CCGTCGTGGG CAGCCCCGCA CTAACCCCAC 1140 GCGCTTCTCT 1150
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