Tag | Content |
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EnhancerAtlas ID | HS111-04158 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr6:3918950-3920090 |
Target genes | |
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: 2 | Chromosome | Start | End |
chr6 | 3919215 | 3919391 | chr6 | 3919432 | 3919937 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I003918 | chr6 | 3918864 | 3920592 |
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Enhancer Sequence | TTGGCCAGGA GGAGGAGTCC ATTCCATTGG CTGGGGTTGC TTAGAATTTG ACTTTTGGTT 60 TACAGCTACA TGGTAGAGCC TATTGCTCCT AGGCTACAAA CCTGTATGTT AGAGGTGGCG 120 AATATCTGAT TTACCGGTGG CAAATCCATA TGGAGCAACC TCAATTCTTG CCTCCTCAGA 180 AGAAAGAATT CAATTGAGGG GTATAAGGCA GAAAAAGAGA CCGAGGCAAG TTTCAGAGCA 240 GGAGTGGAAG TTTATTAAGA AGCTGTAGAG TAGCAAAGAA AGGAAAGTAC CGTTGGAAGA 300 GATCCAAGTG GACACTTTGA AGGTCAAGTG TGGCATTTGA CTTTTTGACT CGGGGTTTTA 360 TATGTTGGCA TATTTCCAGG GTCTTGCATC CCTTTTCCAT GGTTCCTCCC TTAGGGTGGG 420 CTGCCTGCAC GTGTGGTGGC CTGTTAATAC TTGGGAGGTG AGCATGCGCA GTGTGTTTAC 480 TGGAGTTGTA TGCATGCTTG CCTGAGGCTT CCTTCCCTTC CCTGGCGGAA TGTCCCAGGA 540 AGGTCCTTCT TCGCCATTTT GTTTCTTAAT GTGCATGCCT GAGCCTACTC ACCGAATTCC 600 TGAGCTGCCA ATTACCAATT TCAAGTATTT TTTATATATT GTGAAATTGC CTCTCCCTGG 660 GCCTGTGACC AATTATCGCT CTAGTGTGAC AGTTGTGGGC CATCAGGAAA TTGCCTCTCC 720 CTGGCTCCAG CTGCCAATTA TTATTTTTAG AGAGGCACTG TGACAACTGC CTGACTATCA 780 CCTGATGATC ACTTGACATT CCTGGTAGGT GGGGGGAGGG AGCCCTCTCC TGCCCCACTC 840 ATGCCTGGCT AGCTACCTAC TATCACATGT GCAGCATGTT ACTGTGCTGA ATACTATAGT 900 CAATTATAAC ACAATGGCGA GTATTTGCAT ATCCAAACAT AGAAAAGGTA ATGGGTTGGT 960 CTTGGATGTT TCAACACCTA CAACATCACT AGATGACAGA AAACTTTCAG CTCCATTACA 1020 ATCTTATGGT ATTGTTGCAG GACTTTTTCT TAGTTCAGCT AAAGACAGGG TTCTTTGTCC 1080 CATGGCCATA AAAATTCAGG CTTGCAAACA ATTTGAATGG TGAGTAAGAC AGGGTTTTAT 1140
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