Tag | Content |
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EnhancerAtlas ID | HS012-04295 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:68548210-68548900 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr11:68548573-68548584 | ACAGATAAGAA | - | 6.14 | Gata1 | MA0035.3 | chr11:68548573-68548584 | ACAGATAAGAA | - | 6.62 | KLF16 | MA0741.1 | chr11:68548549-68548560 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:68548550-68548560 | GGGGCGGGGC | - | 6.02 | SP2 | MA0516.2 | chr11:68548547-68548564 | CAGGGGGCGGGGCTGGC | - | 6.29 | SP4 | MA0685.1 | chr11:68548546-68548563 | GCAGGGGGCGGGGCTGG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I068780 | chr11 | 68548441 | 68548610 |
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Enhancer Sequence | CACCTACGTG AAACACACAT GTGTGGAACT TAAGTGTTTA AAGAGGCAAC AATGAGGAGA 60 CATTGCACCT CTCTGCTTCA TCCTGGATGG ACTAATTCAC TTTGCACCTG TCCCTCTAAC 120 AGTGAGCAGA CACTCAGTCT CTGTGGAGTG AGGGTGAAAG TACAAACAGG ACACTGAATC 180 ACTCATTTCT TCCCTGTCCC AGACACAAAG ATGAGCGCTT ATATCCTGGC AGCCTGAAGT 240 CAGGACCTGT TGTTATCGCA AGGCAACTGG GGAGAGGTGG GAGGCTCTTC CCGTGGGCAC 300 ATGACCCCTT CATCAGCCAA TCCTTGGCTC CACCCTGCAG GGGGCGGGGC TGGCCAACAC 360 TTTACAGATA AGAAAAAGAG GACTTGAGAT AGCCACATGC CAACACCCTG GCCTAACCCT 420 GTGCCTAGCC CTGTTTGCCA CTCTCCCCTG CCTGAGTCCA GGGACCTGGC AGCCCTGCAT 480 CTCATGAGCA TCTCCAAACA AAGGTGGTCA TGCACAGAGG AGGGAAGAAT CTCAGATTTG 540 CAGCTCAGGC TGTGTATGTG TGATAGTTTT GGCAGAGGGA AGAAAACTGA AGGTTGGCCA 600 GGCGCAGTGG CTCACATCTG TAATCTCAGC ACTTTGAGAG GCTGAGGTGG GTGGATCACT 660 TGAGATCAGG AGTTCATAAC CAGCCTGGCC 690
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