Tag | Content |
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EnhancerAtlas ID | HS101-03596 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:201237520-201238550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr1:201238177-201238191 | ATTCCCCAGGGACC | + | 6.84 | GSC | MA0648.1 | chr1:201237869-201237879 | GCTAATCCCC | + | 6.02 | Nr5a2 | MA0505.1 | chr1:201237750-201237765 | GCTGGCCTTGGACCC | - | 6.24 | ZIC1 | MA0696.1 | chr1:201237692-201237706 | CACAGCAGGGGGCT | - | 6.01 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_26526 | chr1:201237453-201239549 | Esophagus | SE_35843 | chr1:201234594-201238839 | HMEC | SE_37062 | chr1:201234857-201239624 | HSMMtube | SE_64243 | chr1:201234398-201239013 | NHEK | SE_68514 | chr1:201210031-201254923 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 201237679 | 201238422 | chr1 | 201237729 | 201238000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I201265 | chr1 | 201234755 | 201239296 |
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Enhancer Sequence | ATTCCTGAGC CCCAGCCCAG ACCTGGGTGG GCTCCTGAAA TGTCCCTTTT AAAAGAAGTA 60 ATGCCAGATG ATTCTCACGC TCTGTAGTTT GAGAATCATT GGCTGGAACG AAGAGGGCTG 120 ACTAGTGACA AGAAACTGGT CTGGAGGAGT ATGCGGACAT GGCCAGTCTT CTCACAGCAG 180 GGGGCTGTGT CCAGCAGCCT GCAGGGACCC TGCACCACTC CACTCTGTCT GCTGGCCTTG 240 GACCCTCGAC GTGGCAGCCT GCCTTATCTG GGATAAGCTC GTCCTCATCG CAGAATCCTG 300 ATCCAGCTGC CTCAGCAGCA GCTGCTGCAG GGAGGGAGGG CGGTGGAGAG CTAATCCCCT 360 CTGCTTTGGC CCAACACCGA GGCAGAGCCA TCCCCCAGAA CCAGATCCTA CTACGGGAAG 420 AGCCTGACAG GCCATCTGGC TCTTCTTCCC ATCACTGCCA GACTCCCTTG TACCATGGCA 480 CTCCCACGTC TGGGTCCAGG ATGATTCATT CTTCACAGAG GCTTCGTCCA CAGGGAAGTG 540 TCCACATGCA GCGTCTGGGA GAGGGTGGAC ACTGGCTGGT GGCCAGGAGG CCATGTCTGA 600 TCTTGAGAGC CAGGCTGCAT GGAATTATCT GGTAAACGGG GTGCTGTCAT TGTTTTTATT 660 CCCCAGGGAC CAGGCCCCTC CCTTGCTCAA AAGAGTCTAC TATTAGTTAC CTTGGGTCCC 720 AAACACCAGG ATTCTGCGAG TCTACCTGAG TGAGAATCAG GGGCTGGATG TCTGCCAAGA 780 CTCACTTGTC TCTTCTTTTC TCTCTGTGAC TCTGCTTCAT TCTCTCTTTC TCTCTCTCTG 840 AAGCAGGGTT CTCTGTATGC CAGACAACAT GTTAGACAAA TAGGCTCCCC GCTACCCAGA 900 GAGGCTCATT CCCACAGAGT CCCGATTCCA TATTCAGGGT TACTGTTTGG AGCAGTTCAG 960 GTCAGCTGGA CCCCTAAAGG TCCATGTCAC CGTCATGGCT CCTGAATACC AGGGCACGCG 1020 CTTTCTGAAA 1030
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