| Tag | Content |
|---|
EnhancerAtlas ID | HS095-05039 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr11:17399890-17400640 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:17400236-17400254 | AGAAAGGAGGAAGGAAGA | + | 6.04 | | NFAT5 | MA0606.1 | chr11:17400435-17400445 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr11:17400435-17400445 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr11:17400435-17400445 | AATGGAAAAT | - | 6.02 | | POU2F2 | MA0507.1 | chr11:17400557-17400570 | TTATGCAAATGAG | - | 6.44 | | Pou2f3 | MA0627.1 | chr11:17400555-17400571 | CTTTATGCAAATGAGA | + | 7.42 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACAATCCCT CTTAAATGGA TTCCAGTCTT CTTTGTGGAA CTGGTTAGCT CCTTTATTAG 60
GCCCCCTTTT GCTCGTGTGT TTTGTACTAA TGTTTGGACT TTGTATATTC AATACTGTAA 120
CTCAAATTGT TTCCTCTCAC TTAGAGGCTA TTAAACTCCA AATGGTGCTG CAGATAGAAC 180
CACACATAGA CACGCCATTC TTCTGGGGAC CCTTAGACCA ATCTCAGGAG GAGCCCTAAC 240
TGCTGTAACC CCAACGACGC CCCCTTCCAG CAGGAAGCAG CCAGGAGTGG TCATCGTCCA 300
CTTTCCCCAA CAGCAGTTGG GGTCTCCACT CCTGAAGCAG GGAATGAGAA AGGAGGAAGG 360
AAGAAACCAG TCAGACAGGC AGTTAGGGTG GGTCCTCGGT AAAATTCTTC CAAACAAAAG 420
AACAGCTTGA AAAATCAAAC TGCAGGCACA GAGAAGAGAA CTTGTACAGG GAGGCTTGCC 480
TTAGACATGT CCACAGCTGC CTAGGTAAGA AAGACTACAC AGGAGACTTG CCCAGAGATG 540
CCCACAATGG AAAATTCCAT TCCCTGAGAC ATGCGCAGTA AGGGGAACAA AGCCATATGG 600
AGTAACTCAA GCTAAGGGCC TGCATGCACA CTGGGAGGAT AGGGTAGAAC TACCAGAAAT 660
TCATGCTTTA TGCAAATGAG ATGCCCAGCA CTCATCAATT TCTTACAAAA GCCTCTGTAT 720
TCAACTGTGA AATGGCGACA CTCTTTTGGG 750
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