Tag | Content |
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EnhancerAtlas ID | HS101-01254 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:40425450-40426930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:40426047-40426067 | CCCCCACCCACCCCAATCCT | + | 6.6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34178 | chr1:40425200-40426993 | HCC1954 | SE_64654 | chr1:40425188-40426196 | 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 | 40426773 | 40426921 | chr1 | 40426208 | 40426621 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I039959 | chr1 | 40425449 | 40427071 |
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Enhancer Sequence | TACCAAGCAG TGTCTGGGAC ACTAAGTGCT ATGATGACCA CTTCAGGGAA GCTCAGCAGG 60 AGAGCTGGCA TGTGGTCCCT AGTACAGGCC ACACCAGGGG AACTGCAGAA TCCTGGGCTG 120 GGAATTAGAC TTCAGGCCCA GCCTGCTGCA TCTCTACCTC CATGTGGGAC CCTCCAACAG 180 CACAGTGATA AATAATTTGG CACCCCTTCA GGGTGGCTCC TGGCAGAGCA GGGGATGGGG 240 TAATACCCGG AATGGGGTAG CAAACCCATA ACCTTTGGCA CCTTGGATGA CGTAAATTAC 300 CTTCTCCCTT GGTACAAAGC CTGTGCTACT CAGCTTCAGG GGCAAAGTAG GCGGAGGTGG 360 TGCCACGGAT CGGATCAGAC GGCAGGGGAG ACGCACAGGA TAGGCTGTCA GGCGGGGGCT 420 CTGGTTCCCT CCAGGACATC CTGCTTCAGG GTGTGGGGGG GCATACCCCT TTCATCTCCA 480 GCCCATCCAG GCTTAAGTGG GCGCCTTCCT GCCCCAGGGG CGCCCATACC TGGCCTCCGG 540 CCTTCAAAGC TCTTCCCGCA ACCCCTTCCC CCACTACAGC TTCCTTTCCC ACGAGGCCCC 600 CCACCCACCC CAATCCTGCC AGCCCCTGGC TAAGGCCCAG GTTGGAGCCT TTGATCCAGT 660 CTTCAGGGCC GGGGGCAGGA CAGCCTGCCT TACCTGTGCA GGCTGCTCAG GGCTCCCCCG 720 GCGCCAGCCC GTGAGACTTG GCCCTGTGCC CGCCTCCCTG GCAGCCAGTA GAAGGGGAGG 780 CTCTGCTGCC ACGTCGCCTC ATGAGGCCCA GCCAATGGGA GGCAGCCGCT CCCAGGGATG 840 GTGGCTGCAG GCCGGGTTAC TCCCAGTTAC ACTGGGTTCC TCAGCAGCAG CTGCTCAGCT 900 GCTTATGAGC AGAGGATGGA GTGTTTGACA AAGGCTGATG AGGAGCTCTT GTTCCCTGAG 960 GAGACAGAGT CAAGAGAGGT GGAGGTGGGC AGGCCTTCCC TGTGGCATGT AGGAACTGAG 1020 CAACTTCCTG GGCAGGCGTG GCAGCCAGTT TGGGGAAGTT GCTGGGGGCC CTTCAGGCTG 1080 GTTTCTGATC TAGCAGGTGC CTGTGTGCAC ATGCTTCTGT GGCTGGTGGT GCCTGTGTAT 1140 GCCTGCACGC GGGATGGCTC GTGGGCTGAA GGCTGGTGTG CATATGACCT CCCTGTCCAA 1200 ACTTTTTTTC CTTTTTGTGG TGAATGGGGT CTGGCTATGT TGCTCAGGCT GGTCTCAAAC 1260 TCCTGGGCTG GAGCTATTCT CCTGCCTCTG CCTCCCTAAG TGCTGGGATT AAAGGCATGA 1320 ACATCACCAT GCCTGGCCAG ACCTCTCCAT CCATACCACC TGACCCCTCC TCAGGCCAGG 1380 CCTGGAGACC TGGAACCCCC TTTCCTTTCA GTGTAGGAAG AAACTGGGTC TGTCAGGGTT 1440 TGTGAACCCT GTAGCTCTCT CTCCTCCTGG GCCTCAGGGC 1480
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