Tag | Content |
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EnhancerAtlas ID | HS089-10658 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr6:3918970-3919790 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr6:3919448-3919459 | TGCCTGAGGCT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I003918 | chr6 | 3918864 | 3920592 |
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Enhancer Sequence | ATTCCATTGG CTGGGGTTGC TTAGAATTTG ACTTTTGGTT TACAGCTACA TGGTAGAGCC 60 TATTGCTCCT AGGCTACAAA CCTGTATGTT AGAGGTGGCG AATATCTGAT TTACCGGTGG 120 CAAATCCATA TGGAGCAACC TCAATTCTTG CCTCCTCAGA AGAAAGAATT CAATTGAGGG 180 GTATAAGGCA GAAAAAGAGA CCGAGGCAAG TTTCAGAGCA GGAGTGGAAG TTTATTAAGA 240 AGCTGTAGAG TAGCAAAGAA AGGAAAGTAC CGTTGGAAGA GATCCAAGTG GACACTTTGA 300 AGGTCAAGTG TGGCATTTGA CTTTTTGACT CGGGGTTTTA TATGTTGGCA TATTTCCAGG 360 GTCTTGCATC CCTTTTCCAT GGTTCCTCCC TTAGGGTGGG CTGCCTGCAC GTGTGGTGGC 420 CTGTTAATAC TTGGGAGGTG AGCATGCGCA GTGTGTTTAC TGGAGTTGTA TGCATGCTTG 480 CCTGAGGCTT CCTTCCCTTC CCTGGCGGAA TGTCCCAGGA AGGTCCTTCT TCGCCATTTT 540 GTTTCTTAAT GTGCATGCCT GAGCCTACTC ACCGAATTCC TGAGCTGCCA ATTACCAATT 600 TCAAGTATTT TTTATATATT GTGAAATTGC CTCTCCCTGG GCCTGTGACC AATTATCGCT 660 CTAGTGTGAC AGTTGTGGGC CATCAGGAAA TTGCCTCTCC CTGGCTCCAG CTGCCAATTA 720 TTATTTTTAG AGAGGCACTG TGACAACTGC CTGACTATCA CCTGATGATC ACTTGACATT 780 CCTGGTAGGT GGGGGGAGGG AGCCCTCTCC TGCCCCACTC 820
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