| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16467 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr2:74346990-74348140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr2:74347761-74347776 | GGCAAGGGCGTGGCC | - | 6.05 | | ONECUT1 | MA0679.1 | chr2:74347832-74347846 | AGAAAATCGATAGT | + | 6.03 | | ONECUT2 | MA0756.1 | chr2:74347832-74347846 | AGAAAATCGATAGT | + | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGGTAATA TGAACCCATG GATTCTTTTT AATTGAATGT TTTAAATACT TGTCAAATTA 60
TACAAAATTC AACCAACGGC AGCCCCTTCA AACTTATTCC TGTGGCCTTT TGACATTCCT 120
TGGGTGCTTC TGTTTTCTGT TACAGGCCTG AGGTGTCAGC AGGAAAGACG TACTAGTGGC 180
CCCTGAAGCC CTGTTACCTC GGGCCTCTAG GACTTTCGAT AGGCCGCCTC CCTTCTCTTA 240
AGAGCCCACA GGTTGGACCT CCAGGTTCTT CCCTGGGTGC TCCCGGAAGG ACGCTGCTTC 300
GGGCTCCTCC CGGGGGAACT CCATTCTAGG CGCCCGGCTC CCGGCTCCCC CGCCCGCCCA 360
ACCCCGGAGC GCTCCATTCT CCTTGCCAGG CTGCAAACTC CGCCTCCGGT CGCTCTGGCC 420
GACGGCCTCC ACGGCGGCAG GGGGCGACCT CTCGGCAAGA CTTTCCGCCG GGGTCCCAGC 480
CCGGCAGGAG CTTCCGGAGA GATGGCGGGC GACGTCCGTA CCTCTCCGTC TTTCCCTCCT 540
GGGCTGGTGC CGTGGCTACG CCCCGGCCGC TCCACACACC TACCCGGGGG GAACGTGTGC 600
CTGGGCCGCT GGAGTCGCGA ATGGCCGGTT ATTCACACGT TCAAGTACCC AAGGCAGGCG 660
GCCCTGCAGG CGTCGTCGCG GGTTCTTCCG GCCATCTTGT TGAGGAGGGA CCGGAAGGAG 720
GAGCGGCTGA GGAGCCCAAG GAGCGGGGCG GCGGCCACTA GGAGCTCAGG AGGCAAGGGC 780
GTGGCCGAGT GGGACCCACT TGCCTGCCTG GACCCAGAAC TCTGGGATCA GTTTGACAAC 840
TTAGAAAATC GATAGTCTTG AGAAATTCAT CATATCTGCC AAGGAAAGGA CTGAGATTGA 900
ACTCAGCTAT ACAAAACAAC TCAGGAATCT TTTAAAGACA TGCCAACCTA AAAGGAACTG 960
GAAGGAGAAA GAATACATTA CGTAAAACTC TCCTTCCCTC CCTGTGAACA AAATGAGTGA 1020
TCACGCTAGG CAGCATTAAG TTATCTTCTT TGAGGTCTTG AACTTTCAGA TCACCGTGGA 1080
GTTACAAGGG CATGTTCAAA ACCAAAAGCA GGAGAGGAAA TCTCACTTTC ATGATGCCCA 1140
GAAGGCACAA 1150
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