Tag | Content |
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EnhancerAtlas ID | HS047-00640 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:25844160-25845070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:25844756-25844768 | AAACAAACATAC | - | 6.37 | MYCN | MA0104.4 | chr1:25844771-25844783 | GACCACGTGGCG | + | 6.07 | MYCN | MA0104.4 | chr1:25844771-25844783 | GACCACGTGGCG | - | 6.07 | NFYA | MA0060.3 | chr1:25844276-25844287 | GGCCAATCAGA | + | 6.02 | TFAP2A | MA0003.3 | chr1:25844581-25844592 | TGCCTGAGGCT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 25844225 | 25844803 | chr1 | 25844544 | 25844811 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I025518 | chr1 | 25844581 | 25844710 |
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Enhancer Sequence | GCTGCCGTCA GTCGGCCAGT CTCCCACATC TCTGGGACTC CTCTTGCCAC GTCGCAGCTG 60 GGAGAGGCCT AGGGAGAGGG GCTGTGTGCA CGGATTGGCA GTGGGAGAGA GATGTAGGCC 120 AATCAGAATA TCACGCGGGT TGGAAAGGGG GCTACTGTGC GCGAGGTGCC TTCTCGTGCC 180 CTGCCTCAGT GGGACCCTCA CCTTAGCTCC GTGCAGGTGA GGAGGCTGGG CCTGGGCCAA 240 GCTCTCACAG CTACAGGGTG CTGGGTGGAA GGGGGCCTCC TGCACTCGGA GCTCTTGGCT 300 TGTCTCCACC CAGCAGCTCC CTTGAGGAAG GTGGGGAAGG TCGCAGCTTT GTGCAAAGGG 360 AGCGAGTACA CAATGTGGCC GCCTCCTCTT TTCCATCCCA TCACCTCTCA TTTCACCAAC 420 CTGCCTGAGG CTGCAATCAA CACTCCCCGC GTGTGGGGGC GGAGCCAACC CACGAGGCCA 480 TGCTTCAGGC CCCTGATTGG TTCAGGAGTA GCGCTTGACC TAATGAGGCG CTACCAATGG 540 GATGCAAAGA GACGTTCCCT GGCCTTCTGC CAGAGCGGTT TCCCTGTTCT CCCAACAAAC 600 AAACATACCT GGACCACGTG GCGCGAGGAT ATTAAGTTTA AGATGGTGGC AGCAGTTTTT 660 GAGACCTTGC AGAGAGAGCT GCTGAAAGCT GCTGGGGGCG CAGCCTCTCA GGTTGTACAC 720 GAGGTGCTGA GGTTTTTTGT TTTTAATTTA TGTATTTATA TGTATTTATT GAGACGGAGT 780 CTTCCTCTGT CGCCCAGGCT GGAATGCAAT GGCGCCATCT CGGCTCACTG CAACCTCCGC 840 CTCCAGGGTT CAAGTGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAT TACAGGCTCC 900 CACCACCACG 910
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