Tag | Content |
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EnhancerAtlas ID | HS053-00541 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:20451060-20452040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:20451526-20451537 | GGGCGGGAAAG | + | 6.32 | FOSL1 | MA0477.1 | chr1:20451172-20451183 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr1:20451172-20451183 | GATGAGTCACT | - | 6.32 | ZNF740 | MA0753.2 | chr1:20451098-20451111 | GTGGGGGGGGTAC | - | 6.39 |
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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 |
GH01I020124 | chr1 | 20450852 | 20452009 |
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Enhancer Sequence | TTAGACCACA GCTCTGCTGG AGCCCGCCTT ACTGTGGGGT GGGGGGGGTA CTGCCCTAAG 60 AACTCCACAT ATAATAAGTC TAAGTAGGTA CTGTCATAAT CTCCATTCCA TGGATGAGTC 120 ACTGTGTCTT GGAGCACTGC CATATGAATT CTCTTACCCG CCCAGCATAG ACAACCGTGA 180 AAGCCAGAAG AGCTGGCAGA GTCTAGAAGT TGGCTGCCCC CACCCTCGCT GCAGACCAGA 240 AGAAAGTGGA CCCTCTTTCT CACTTCCTAA GAATACCCCC CTAGGTGACA GCACATCCTC 300 TCAGCCCATG GCAGGAGACC TCCCGTGCAA AGCCCTGTTG ACCAGAAGAG TCCCATTGCC 360 CGGGTTCCAT TCACCATGAA AGCCTGCCAG AGTGTATCTG AAATGAAGCT CCAAATTCCC 420 ACAGGTTTGC AAGATCAGAG GGAAGCAAAG GAGAAGGGCT TCCCCAGGGC GGGAAAGAGG 480 GAGGAGGGAG AGATTAGCTT TTGTGGGAGA GTGACCCACT TTTCTCCACC TGAATCAAAG 540 GAAATGGATT AAACGAGAGT CCCCCCAAAT GCCTGTCAAC AGTAGAATGG AGAGACCTGT 600 GGCGGTATAG TCAACCGATG AGAACACCAT GTCAACAAAC CACAATGACA CACAAGGACA 660 TGGATGAATC CCACAAGCAT AGAACGAAAA ATAAAGCCAG ACACAAAAGA GCACAGAGTG 720 TGAGACTCCA TTGCTACGAC GTTCCACAAT ACTCAAGCTC ATGTGTGATT TCACAAGTCA 780 GGACAGCGTT CCCCACGGCT GTGCATGCTG ATTAGAGGGG GTTACTAGAG GTCTTCCTTC 840 AGGCAGTGCT GCTGATGTTC TGTCTGTTTG GTGTTGGTTA CATGGGTGTG TTCGCATTGC 900 AATAATTCAT CCCGCTGTTC ACTAAGGTTT GTGCATTTTC CTGGATGTAT GTTACATTAA 960 CATGCATTTG AATGATAATA 980
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