Tag | Content |
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EnhancerAtlas ID | HS184-32281 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chrX:62653960-62654990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chrX:62654450-62654468 | GAAAGGGAGAAAGGAATG | + | 6.21 | NFAT5 | MA0606.1 | chrX:62654775-62654785 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chrX:62654775-62654785 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chrX:62654775-62654785 | ATTTTCCATT | + | 6.02 |
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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 |
GH0XI063433 | chrX | 62653039 | 62655310 |
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Enhancer Sequence | ATGGAGAAGA GCCGGGGTGC CCCCGTAGCT CTTCGTGGTC CCCCAGAAAC CAGAGTGGTC 60 AGAGCGTGAG CATTCTGAGG GCATCCCCTG AGAAGGCAGG CCAGGGTCAC CCAGTGGTGA 120 CCGGGGAATC CTCTTACCTG GCGCTGGGGT TTTCTGGCTA ACAGGCAGAA ATATGAGAGG 180 AATCCAGAGG GTGGAAAGGG AAACTCACCC ACAATTGGAG GCCGGTGTTG GATGCAATGG 240 GAGTGGTCCT TGCCAGAGCC ACAGAGAGGA AAGAGGGGGA AGGAGAAAGC GGTGGGAGGA 300 TGGGGCCGAG AGAAAGAATT CCTCCGTAGA AAGACGAAAG TGGGCAGGGC TGGGAACCAG 360 GGGCCAATCA GGATTTGGGA ATTAGCCCGG GGCGAGCTGC CGCTGCCTCT TCCTTCCCAG 420 GTTGCAAGGA AGTACCTCTC CCTTGTGGGA TCTAGACCCC ATCCCAGGTT TTGGCACCAA 480 ATGTTAGAAC GAAAGGGAGA AAGGAATGGA GCAGAGGCAG CTCAAGGGCA ACACAGGTTT 540 ATTGGGAGAA AGGCCTGCAG ATAGGGGGTA CTAGCTAGCG TCGGAGCCCC AGTCCTTCTT 600 ACAGGCTGGG GCAGTTCTAG GCCTGGGCAG GAGAGGTCGG GGATGGTTGA GAAAATGGGG 660 CGGGGGTGGT GTGTTTGGCT GCTGATAAAG GAAGGAATTT ACTGCAGTCA GGGGTTAGGC 720 CTGGAACCTG TCTGACAGGA TGAATTTATT GCCCTCAGGG TTTAGGCCTG GGACCTTTCC 780 AACAGGATGT TTCTCACAGC TCAGGCGCTG GTGGAATTTT CCATTCTGAC CAGAGTTTGT 840 AAAATGGTGG CAGTCTGCAA AATGGCGTGG CTTGGGCTAA CACGATCAAC ATGCATCAAT 900 TTCACAGACA AAATATTGGG CGGAACACCC CAGGATAATA CACAAAATGA AACTGTTTTG 960 GTAAATACTG AAAACATGCA AAACAACATA AATGTTATTT TTATATACTA AAATATGTAC 1020 TAGGATCTTA 1030
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