Tag | Content |
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EnhancerAtlas ID | HS007-05138 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr14:76383350-76384860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr14:76384787-76384799 | GCTATAAATAGA | + | 6.62 | MEF2B | MA0660.1 | chr14:76384787-76384799 | GCTATAAATAGA | + | 6.52 | ZNF263 | MA0528.1 | chr14:76383362-76383383 | GGGGGTGGGGAGAGAGGGGAA | + | 6.1 |
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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 |
GH14I075917 | chr14 | 76383841 | 76383990 |
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Enhancer Sequence | TGGTGGTCAG CAGGGGGTGG GGAGAGAGGG GAATAGGATG TTTTTGTTTA ATGGGCACAG 60 AGTTGCAGTT TTGCAGGATG CAGAGTTCTG GAGCTGAATG ATGGGATGGT CGTGCAGCGT 120 GAATGCACTT AATGCCACTG AACTGTACAC TTGAAATTGT TAGGATGGTA AAGTTTATGT 180 TACATGTATT TTGCCACAAT TTTTAAAGAA AGATTATAGA TTGTGTATGT ATTATACCCC 240 AGATTAGGTG TTTTTGTTTT CTCGATTTTG CATTTGAGGA AACTAAGGCT GAGAGAAGTT 300 AAGTAGCTTG TCCAAGCCAC ACGGTCAATG ATGGAGCTGA AATTCACACC CAAGCAGTTT 360 TTTTCTAGAA GCTGCTGAAC TGCTTCTTCA TCTGAAAACT CGGCCCGTCA AGGTGATTTC 420 ATTTTATCAG CTTCCTTTCC TAATGGAGCT AAGCGGCTGG TGATCAGGCC CTGTGGCCTC 480 CGCCTCCCTG CAGTGTCTGG TTGTTATCTC AAATGGCTCA TTAGGGGGAT GCCTGGCAGT 540 AGGGGGGCAT GTGTAGTTTA GGCTGGCTGT CTCTTTATCC AGCCATTTAA CTTTCTCTTA 600 TTTAGATGGA GCCAGACCTG GAGAGGGAGG ATAAGGAGCA AGGTGGGCCT TCTGCCTCTA 660 CTCCCCTGGG TGGGGGTGAT CTGGGATCTT TCCCACATGC CCGAACCGCC TTCGAAGGGA 720 CAGCAGTTCT GGTTGGCAGA GGAAACATGG ATGTAGATGA AGCTCTGCAG CAGAGGGTGG 780 AGCTGAAGTG AGGAGGTAGG AGGTGGGGGA AAAGCCGAGA GGGCTTGGGA ATCACCCCTG 840 GATTAGTTAA GAGAGCATTC CCTGCAGGTA ACAGAAACTC CGAGAAATCA GTGGCAGGGT 900 AAGTAAGGGA TTTATTTTTC TCACATGTCA AAAAGTCTGG AGACAGGAGG TCCAGGGCTA 960 GTGCTGCTCT TCAGAGACAT AACTGAGGAG CCAGGCTGCT CTCTTTCTGC TCTACTAACT 1020 CTAATGCATT GGCTTTCATT TTGCTGGTCA TAAGATGGTT TCTGTTCCTA CCGGCATTGT 1080 GTCCATGTTT CAGTGAGAAG AGGGGGAAGG GCAAAAGACA GATGCCAGGT CAATCTGTCC 1140 CCCTTTCAAA AACACTTTCT TGGAAGCCCA GCAGTTCTAA CTACCATATC ATTGGCCAAC 1200 ACTGGCTCCC TTGCCTACTT CTCCTTAGCA ACAGAGGTGT CTAGAGAGGT GGTCTTTTAG 1260 CTGGGCACAT TGCCTTCCCA GTCAGATCTG GGCTCTTTTA TTGAGGAAGA AGGGGGGATG 1320 GCTAATGATA TACATCTACT GGTTTCAATC ACAGCACATT TTCTTTCCAG AGACTCCACC 1380 CCTGCTGGAG GAACTTCATC ACACTTCTGC AGCCCCTCTA CCACCAGCTT CTTGACTGCT 1440 ATAAATAGAT ACGTTGTTCC TTGACCCAAA TTTGCCCCAG TCCTGTCTAC TAGTACATGG 1500 AGTTGGGGGT 1510
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