Tag | Content |
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EnhancerAtlas ID | HS095-00766 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:33404940-33406240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:33405375-33405386 | TCTGACTCATT | + | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23323 | chr1:33404962-33406888 | Colon_Crypt_1 | SE_35956 | chr1:33404029-33406655 | HMEC | SE_64575 | chr1:33405302-33406177 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 33405191 | 33405597 | chr1 | 33405125 | 33406004 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I032939 | chr1 | 33404746 | 33408136 |
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Enhancer Sequence | ACCACACCCA GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTTACCAT GTTGGCCAGG 60 CTGGTCTTGA ACTCTAAACC TCAGGTGATC ACCCACCTAA AAAAGGTGCT GGGATTACAG 120 GCGTGCGCAG GCCCTGCCTA CTTATTATTA TGCATCTCTC ACTTGTCTGT TAACTCCACA 180 AAAGGAGAGA CCACAACTCA TACACACTTT ACCTTCCCTG CCTTGCACAT AATAGGAAAT 240 CAAACATTTA ACAATCAAAT TACCTCCAGG GAATGAGACT GAAGGACATA CAGGAGCCAA 300 CCTCTTCCCT CCTCTTGGAG CAGCAAACTT TCCCAATAGT GTCTCAGAGC CCATAACTAT 360 TGCCTTTCTT GGCTCCAACA TCACTTTGTT GCACAGTTAA GTATTTCCTT ATAATGGGTT 420 TCACAGTCAA ACCCATCTGA CTCATTCACT TCCTATAAAA TAAAGGCTTT CACAGAACTA 480 GAACAGCTGG ACTGGCTAAG CTGCAGTTTC AGCAAGTCAG TCTCCAATTA TGTCTGTCTG 540 CTTATTTACA GGGGTGTTGG TTTTAAGAAA GCACAGCAGT GAATATGCCA GCATGTGGGG 600 GCGGGATCCC CTGATAAGAG ACAACCAGAG TCATGAGATG CACAGACGGG TCAGTAGCAG 660 CCTGCAGCTG CACATTCAAG CAGCTTCCAT CCTACTGCCT GAGCCTTTGC TTTGCTGCTC 720 CAGCTTCAGG TGCCCTTCAA AAATGTGCCA AGGCCCAGGG AAATGAGGGA ATGCAATGGA 780 AAGTGCACAG TGTCAGAGAC CTGGCTTCTA GTTTCAGGTC TGCCACAGAA TCACTCTGAG 840 TTGGAAGAGT CTTTCAGAAA GGGCTCCTAC TTAGGTGGTT GTCAGATGCT GGTTCATGCA 900 ACGGCTGTGC TAGAATTACC TGGGGAGCTT TTGCAAAACA CGGATCACCC CCTAGGTGCC 960 ACTCCAGGAA ATTCTAAGCT ACTCATTCTG GGATGGGTCC CTGAAGTCTA TTTTTAAGAG 1020 GCTCCCAAGT GATTGACAGG CACTCAGGTG GGAGATCCAG TCCACCTGCC ATCTGTTGCT 1080 TGAATCCTTC TTATAGCCAA ATAGCCATCT GGTCTCATTG TAAACATTTC CAGGGATAGG 1140 CAGCTCAGTA TCTACTAAAG TAGCCTTTTT CCTCTTTGGG CTTTCATGTT GCTTTTCCCT 1200 ATATTCTCTA TACTGAACCA AAATTAGTTT CCCTTTAGCT TCTGCCAAGT CATCTTAATC 1260 TACCTTTTGG TATGAGGCAT AGAAGTCTAA TCCTTTTCAC 1300
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