Tag | Content |
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EnhancerAtlas ID | HS002-00259 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:33405010-33406190 |
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 | ACTCTAAACC TCAGGTGATC ACCCACCTAA AAAAGGTGCT GGGATTACAG GCGTGCGCAG 60 GCCCTGCCTA CTTATTATTA TGCATCTCTC ACTTGTCTGT TAACTCCACA AAAGGAGAGA 120 CCACAACTCA TACACACTTT ACCTTCCCTG CCTTGCACAT AATAGGAAAT CAAACATTTA 180 ACAATCAAAT TACCTCCAGG GAATGAGACT GAAGGACATA CAGGAGCCAA CCTCTTCCCT 240 CCTCTTGGAG CAGCAAACTT TCCCAATAGT GTCTCAGAGC CCATAACTAT TGCCTTTCTT 300 GGCTCCAACA TCACTTTGTT GCACAGTTAA GTATTTCCTT ATAATGGGTT TCACAGTCAA 360 ACCCATCTGA CTCATTCACT TCCTATAAAA TAAAGGCTTT CACAGAACTA GAACAGCTGG 420 ACTGGCTAAG CTGCAGTTTC AGCAAGTCAG TCTCCAATTA TGTCTGTCTG CTTATTTACA 480 GGGGTGTTGG TTTTAAGAAA GCACAGCAGT GAATATGCCA GCATGTGGGG GCGGGATCCC 540 CTGATAAGAG ACAACCAGAG TCATGAGATG CACAGACGGG TCAGTAGCAG CCTGCAGCTG 600 CACATTCAAG CAGCTTCCAT CCTACTGCCT GAGCCTTTGC TTTGCTGCTC CAGCTTCAGG 660 TGCCCTTCAA AAATGTGCCA AGGCCCAGGG AAATGAGGGA ATGCAATGGA AAGTGCACAG 720 TGTCAGAGAC CTGGCTTCTA GTTTCAGGTC TGCCACAGAA TCACTCTGAG TTGGAAGAGT 780 CTTTCAGAAA GGGCTCCTAC TTAGGTGGTT GTCAGATGCT GGTTCATGCA ACGGCTGTGC 840 TAGAATTACC TGGGGAGCTT TTGCAAAACA CGGATCACCC CCTAGGTGCC ACTCCAGGAA 900 ATTCTAAGCT ACTCATTCTG GGATGGGTCC CTGAAGTCTA TTTTTAAGAG GCTCCCAAGT 960 GATTGACAGG CACTCAGGTG GGAGATCCAG TCCACCTGCC ATCTGTTGCT TGAATCCTTC 1020 TTATAGCCAA ATAGCCATCT GGTCTCATTG TAAACATTTC CAGGGATAGG CAGCTCAGTA 1080 TCTACTAAAG TAGCCTTTTT CCTCTTTGGG CTTTCATGTT GCTTTTCCCT ATATTCTCTA 1140 TACTGAACCA AAATTAGTTT CCCTTTAGCT TCTGCCAAGT 1180
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