| Tag | Content |
|---|
EnhancerAtlas ID | HS184-21937 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr3:183734530-183735610 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:183735323-183735342 | CAGCGCCCCCTGGCGGCCG | - | 7.53 | | EWSR1-FLI1 | MA0149.1 | chr3:183735384-183735402 | CCTACCTGCCTGTCTTCC | - | 6.29 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCCAAAGAA GTGCCCAATA GGGTTGAGGC CACTTAGTCA GCTGCCCTTT TTTACCAAGA 60
TTCTCTTTCC ACTGATAAAA GTGTAGACAC TCTCCCTGCA CAATGATACT GATTCAACTG 120
CATGGCAGGA GGAGAGTTGC ACGGGATTAC CAGACTGGTG TGTGCAAGCT GCAGTCATCC 180
CAACACTCAT GAGTAGGTTT CCATCACCTC CAGGCCCTCA AGCTGCACGA GGAAGACACC 240
ACGCTAAAGG GATACGTATT TACCACACCC ACTGTAATCC ACTTGTTGCG TCTCCAAGCA 300
GCCTCACCTT TCATACACGC TGCGGACCAC AGTAAAACCT AGCCATCTCC TCCTCCAAGA 360
CCTCCTGAAA CTTTCCCCGT CGTTCCTGTG CCCACCTGCC TCCAGCCTCT CCGTCTGTGC 420
AGAAACCAAA TGGCCCCTGT GTGATAAACA CAAAGCCACC CGCGGCTCTG TGTGGCAGAA 480
GCGAAAAGAG CACTGGATGA CCGTGGAGAG ATCTGGGCTG CGTTCCCGGC ACAGCCACGG 540
CTTTGCTGCG CGTGCTTATG TCACGTACCT CCATTTACCC GCTTGCAAAA ACGAAGGGGA 600
TGACTTACTT CGAAGGTCGC TGGCGGCTCC GCTGCGGGTT GAGCAGGGTG CCCCGAGCCA 660
CCCGCTGCAC AGCCTCCCAG GTGGGCGTTT CTCTCAGACC CGCTTCGCCT GGGATGCCCG 720
GGCCCTAGGG CGTTCCCACA GCCCGCTCCG GCCTGCCCAG GCGAGCGCGA CCCACACCCA 780
CGGCCCGCGG GCGCAGCGCC CCCTGGCGGC CGCGGCCAGG GACGTAGCCC GCGTCCCTGC 840
CCGCTCATCC CGATCCTACC TGCCTGTCTT CCAGCACACG ACCCCGTCAC CAGACCCCGG 900
GCTCACAGGC CTAGGAGGCG GCGGCAGGAG ACCAGGGGGA GGCCATACGC CGTTCCCCAA 960
GTCTCCAGTG TCCCCCGAAC TGCTCGCAGC CCTGGCCACA TCCCGCCACG CCCCGAGGAA 1020
ATGCAAAGGG GTGATCCCCG TGACAACCGA GCTGGAGGGC AGGGGTGCGG CAGCAGCCAT 1080
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