Tag | Content |
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EnhancerAtlas ID | HS184-19310 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:29865700-29866810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:29866570-29866589 | TCGCCTGCAGGGGGCGCTG | + | 7.1 | MAFF | MA0495.3 | chr22:29865912-29865927 | GTGCTGACGCAGCAA | - | 6.32 | MAFF | MA0495.3 | chr22:29865912-29865927 | GTGCTGACGCAGCAA | + | 6.37 |
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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 |
GH22I029469 | chr22 | 29865790 | 29867110 |
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Enhancer Sequence | ACCAGACAAG GCTGTGGGAG GGGGAAATAA TGCATGTGAC TGGCCTTCAC ACAAAGCCAA 60 GCACATAGTC AGTGCTCAAT AAATGCGGGC TACTACTGTT ACCAATTACT TCCACAGCCA 120 TGTCTCATGT CTGTCACCAT CCCAGACTGC AGGGAGTCTG GTCCACCAGC AAGTGGCCGG 180 TCCCCAACCT CCAGGGCTCT CCAGTCTCAA GAGTGCTGAC GCAGCAAGGG AAGGAGCTCC 240 CAGTACATCC ACACCGGCTC TCCTGACTCA GCTCTGATTT CTCAGGTGCC TGTGTAGGGT 300 CGACAATTCT GAGCATGCTG GACGAAATCC CGATTTTTGC ATTCATGTAA GAGTCTTGGA 360 AGAGCCCCCT TTTCACACGT GCAGAAACTG AGGTCTGGGG AGGAGGAAGA GGCTGCTGCC 420 CACGGACACA CAGGTGCCAG GACCAATGTC TGGGGAGGAG GAGAAGGGCG CTGTTCACGG 480 AAACACAGGC GCCAGGGCTT GATGCACCGG TGTCCTCGCT TGTGGCTGGG TCCTTCTGGG 540 ACGATCCCCT TTCCCAGGAT CCCGCCCCTA GGAAGAGCAC CGGCCATGCC CCTACCTGAG 600 CCCCACCCCC TGAGTTCTTT GAGCACCGCT GCCCCCAGGC CGTTACGATG AGGGAAGCCA 660 CGACAGCCAA GGCTACGGCT ACCTTCCTGC AGCCCCTGGG GATGCCACTG ATGCGACGCC 720 GCGGCGGCCA AGGCGGGGCT GAAGGCGGCG CGCCCGGCTT CCCTGAGCCA GTTTGGAGGA 780 GCGCTCTTCA ATCTTCCGAG GCCGGATGAA GCATTCGGGC GTTCCCACTG CGGAAGGGCG 840 GGGATGGCTG TGACGCAGGC GTGCCCGCCG TCGCCTGCAG GGGGCGCTGT TGCTGGCGCG 900 ATTCTATCAA GCGCAGAGCC AGCCGAGGCA GTATGCCGAG GCAGAGAAAC CGGTTCTGCA 960 GTCCCAGGGC CTCGGTTTCC CCCTCTGGAG AGTGTTCGTT TGTGACAGGG TCTCGCTCTG 1020 TTGCCGAGGC TGGAGTGCCG TGGCGTGATC TCGGCTCACT GCAACCTCCG CCTCTCCAGG 1080 TTTAAGCGAT CCTCCCACCT CAGCCTCCCG 1110
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