Tag | Content |
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EnhancerAtlas ID | HS187-00586 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:33405000-33406430 |
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 | CTGGTCTTGA ACTCTAAACC TCAGGTGATC ACCCACCTAA AAAAGGTGCT GGGATTACAG 60 GCGTGCGCAG GCCCTGCCTA CTTATTATTA TGCATCTCTC ACTTGTCTGT TAACTCCACA 120 AAAGGAGAGA CCACAACTCA TACACACTTT ACCTTCCCTG CCTTGCACAT AATAGGAAAT 180 CAAACATTTA ACAATCAAAT TACCTCCAGG GAATGAGACT GAAGGACATA CAGGAGCCAA 240 CCTCTTCCCT CCTCTTGGAG CAGCAAACTT TCCCAATAGT GTCTCAGAGC CCATAACTAT 300 TGCCTTTCTT GGCTCCAACA TCACTTTGTT GCACAGTTAA GTATTTCCTT ATAATGGGTT 360 TCACAGTCAA ACCCATCTGA CTCATTCACT TCCTATAAAA TAAAGGCTTT CACAGAACTA 420 GAACAGCTGG ACTGGCTAAG CTGCAGTTTC AGCAAGTCAG TCTCCAATTA TGTCTGTCTG 480 CTTATTTACA GGGGTGTTGG TTTTAAGAAA GCACAGCAGT GAATATGCCA GCATGTGGGG 540 GCGGGATCCC CTGATAAGAG ACAACCAGAG TCATGAGATG CACAGACGGG TCAGTAGCAG 600 CCTGCAGCTG CACATTCAAG CAGCTTCCAT CCTACTGCCT GAGCCTTTGC TTTGCTGCTC 660 CAGCTTCAGG TGCCCTTCAA AAATGTGCCA AGGCCCAGGG AAATGAGGGA ATGCAATGGA 720 AAGTGCACAG TGTCAGAGAC CTGGCTTCTA GTTTCAGGTC TGCCACAGAA TCACTCTGAG 780 TTGGAAGAGT CTTTCAGAAA GGGCTCCTAC TTAGGTGGTT GTCAGATGCT GGTTCATGCA 840 ACGGCTGTGC TAGAATTACC TGGGGAGCTT TTGCAAAACA CGGATCACCC CCTAGGTGCC 900 ACTCCAGGAA ATTCTAAGCT ACTCATTCTG GGATGGGTCC CTGAAGTCTA TTTTTAAGAG 960 GCTCCCAAGT GATTGACAGG CACTCAGGTG GGAGATCCAG TCCACCTGCC ATCTGTTGCT 1020 TGAATCCTTC TTATAGCCAA ATAGCCATCT GGTCTCATTG TAAACATTTC CAGGGATAGG 1080 CAGCTCAGTA TCTACTAAAG TAGCCTTTTT CCTCTTTGGG CTTTCATGTT GCTTTTCCCT 1140 ATATTCTCTA TACTGAACCA AAATTAGTTT CCCTTTAGCT TCTGCCAAGT CATCTTAATC 1200 TACCTTTTGG TATGAGGCAT AGAAGTCTAA TCCTTTTCAC AGTTGAAGGT CCTTTGGATA 1260 GCTGAAGGCA ACCATCTCCT CTACCTTCCT ATCCTGCTTT GTTCTACCTT TACCCCTCCC 1320 TAGGCCTTTC TTCTCCGTTG CATTCAACTG CTTCTCAGGC AACATGTTAT GCTCCTCTGA 1380 AAATATACAC TCTGGTCTGC CTAACTAGTG AAATGACCAA GCAAGTCACA 1430
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