Tag | Content |
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EnhancerAtlas ID | HS094-00662 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:33404730-33406060 |
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 | ATTATCCCAG CAAACCATTC ACTTCTTGCT AAGTACTCCC ACAGCACCTG CCTACTTATT 60 TATTATTATT TGTTTTTAGA GGGAGTCTCA CTCTGTCACC CAGGCTGGAG TGCAGTGGCA 120 CGATCTTGGC TCACTGCAAC TTCTGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT 180 CCCAAGTAGC TGGGATTATG GGTTCCCACC ACCACACCCA GCTAATTTTT GTATTTTTAG 240 TAGAGATGGG GTTTTACCAT GTTGGCCAGG CTGGTCTTGA ACTCTAAACC TCAGGTGATC 300 ACCCACCTAA AAAAGGTGCT GGGATTACAG GCGTGCGCAG GCCCTGCCTA CTTATTATTA 360 TGCATCTCTC ACTTGTCTGT TAACTCCACA AAAGGAGAGA CCACAACTCA TACACACTTT 420 ACCTTCCCTG CCTTGCACAT AATAGGAAAT CAAACATTTA ACAATCAAAT TACCTCCAGG 480 GAATGAGACT GAAGGACATA CAGGAGCCAA CCTCTTCCCT CCTCTTGGAG CAGCAAACTT 540 TCCCAATAGT GTCTCAGAGC CCATAACTAT TGCCTTTCTT GGCTCCAACA TCACTTTGTT 600 GCACAGTTAA GTATTTCCTT ATAATGGGTT TCACAGTCAA ACCCATCTGA CTCATTCACT 660 TCCTATAAAA TAAAGGCTTT CACAGAACTA GAACAGCTGG ACTGGCTAAG CTGCAGTTTC 720 AGCAAGTCAG TCTCCAATTA TGTCTGTCTG CTTATTTACA GGGGTGTTGG TTTTAAGAAA 780 GCACAGCAGT GAATATGCCA GCATGTGGGG GCGGGATCCC CTGATAAGAG ACAACCAGAG 840 TCATGAGATG CACAGACGGG TCAGTAGCAG CCTGCAGCTG CACATTCAAG CAGCTTCCAT 900 CCTACTGCCT GAGCCTTTGC TTTGCTGCTC CAGCTTCAGG TGCCCTTCAA AAATGTGCCA 960 AGGCCCAGGG AAATGAGGGA ATGCAATGGA AAGTGCACAG TGTCAGAGAC CTGGCTTCTA 1020 GTTTCAGGTC TGCCACAGAA TCACTCTGAG TTGGAAGAGT CTTTCAGAAA GGGCTCCTAC 1080 TTAGGTGGTT GTCAGATGCT GGTTCATGCA ACGGCTGTGC TAGAATTACC TGGGGAGCTT 1140 TTGCAAAACA CGGATCACCC CCTAGGTGCC ACTCCAGGAA ATTCTAAGCT ACTCATTCTG 1200 GGATGGGTCC CTGAAGTCTA TTTTTAAGAG GCTCCCAAGT GATTGACAGG CACTCAGGTG 1260 GGAGATCCAG TCCACCTGCC ATCTGTTGCT TGAATCCTTC TTATAGCCAA ATAGCCATCT 1320 GGTCTCATTG 1330
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