| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10366 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr14:76308580-76309840 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:76309062-76309080 | GGAAAGGAGGGAGGAAAG | + | 6.42 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCCACACCC TTGCCAGCAT TACATACCAT TGACCTTTCT GTCTATTCCT CTGGACTGTC 60
GCTCTCCCAC TTTTACTGAT GATGAAATGA GGAGTGGACC CTATCTTCAG ATATATTACT 120
TCAAGGGTGT TTTGTTTGGG GCAGGAGTAC AACTGAGAGG AGGCCGAGAA GCAGGAGGGT 180
AAAGGGTTCT CCGTGGGCTC TTTATTTTCT TAATGTTCCT TAAGACTAGA AGGAATCCCT 240
GTGAGTCAAG TTCATCTTCC CTCCACGCTG CTTAGGTCTT TTCTCTCCTG GTTTTGTTTT 300
TGATTGATTT TACCCAGGGA GCCTGATCCT CTCCCCTTCC TAAGTAATGA ATAACCAGAA 360
AAAGTTATAG AACCCAGCAA ACTGAATGAA AAAAGCTTAA GGAAAATATT AAAAAGGAAG 420
AAAAGTGTTT GATGTACTTT TAATGTAAAA TGTGGAAAAA GTAGAAAATG GGTGGGGGTT 480
GGGGAAAGGA GGGAGGAAAG AGATTATTCA CGGTAATGGG AACCAAATGT TGGCTAGGAA 540
AGCTGCAGTA TTCTCACACT CTTCCTGTAA ACCCAGCGGC TTTTCAAAGT GATAATAATC 600
AAGGGCTGAC AGCACAGGAC ACGCCTTAAC CCTTCCATAC CTGGACACTT CCTTTGAGTC 660
AGCCTCAAAG GTGGTGTCCA CTTTGAAGAA ATCCTGGTAT ATTTCAGTGC CCTTTTTGCC 720
TCCATAGCAA AAAGAAGAAA GGTGGAGGCA AGTTTTGAAC AGCAAAGCAC CTGCTTGCTA 780
AAACTCCTTT CAGTATGCCC AAATTTCTTT TCTGTGGACA GAGAGCAGCC TGCCTGACCA 840
GTCCAGGATA TTTTCTCCCC TTGCTGTCCT GAGAGGAACT TGAAAGGAGT TGAGAACCTC 900
CTTGTGACAG ATAGGATTCT CTTTCCATCA GTAATAATCG CGTTTACTTG AAAACCCTCT 960
AGTCTGAAGC CCTCCTAGAT GCCAGTGTGG AAGTGCATGC ACTTATTTGG AGGCTTAGAC 1020
CTTTGTTTCT CTTGGAAGTC CACTCTTCCC ACTGTGGAAC TGAGATGTAA ATATACTGTT 1080
CAGAGCTGAA GGGCTCCCTG AGCTTATGAC TTCCAGCTGG TCAAGAACAG TCATATGCCT 1140
CTTGGCCTAA CCATTCATCC AAGGAGGGAG AAGGAAAGGG GGTTACTAAA TGAAGTTCCT 1200
GGTTCAGCTG GATCTTCACA TCCATCTAGA TTTAAACTTT GTTGAGACAC CTTTAAAAGT 1260
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