| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14220 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:136267000-136268000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr9:136267067-136267087 | TTGGAAGGGTTGGTTTGGGG | - | 6.45 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 136267140 | 136267239 | | chr9 | 136267415 | 136267544 |
| Enhancer Sequence | ACCCAGGGTG TGTCTGCCAG CCACCTCCTG CCCCACCCAC GCTCCAGGAC AGCCCTTCCC 60
AGGGGTCTTG GAAGGGTTGG TTTGGGGTAT AGGTGGGTTG GACAGGACAG TGCTGGGCCT 120
CCTCCTGAGA TACATGGTGG CATTTGGCCG TCTTCATTTG GCCACCCCAA ATGCTGGTCG 180
CATCCTTTTC CATCTTGATG ACAAGCTTCC ACTCTTGAAG TCACTGGTTC CCTCTACAGA 240
CATGCTAGGC GCAGCTGTGG GCTTCACACC AATGACATCT CTTTCCCACA CTTCCTGCCC 300
CTTCTGGGAG GCTGGGGCTC AAATGCCCTG TGTGTCTCCA TTCCATAGGG CCCAGTGGGC 360
TTCCGAAGCC GCCAGCCAGG ACTGTGGGAA GGAGAGGGCC ATACAGAGCG CTCACACCTT 420
CACCCACAAA TCGGGTGGGC ACTGTTCTCC CCAACAGGAA GCTGGGCCTC GAGAGAGCCT 480
AAGGACAGTT GCCAGGAGTC CATGCAGCAG GGTTCAGGGC TGGGGTCTGG GCCCCAGCAC 540
CCTCTTTACT GCACAGACTG GATAACTGAT GATACATGGC TGATCTCACT TTGGGGAGTG 600
AAAGGAGGCA CTAGGAATAG ATGTCAACTG GAACCCTCAG GCAAAATGGA TGTCAGTTCA 660
TCCTACCGGG ATAGGGCCCC GTCATGGTTC CATCCTGGAA GGCACAGGCT GGCTCTGTGA 720
GCCCAGGAGG CAGGGTCAGG CCCCCTGGAT GGGAAGCTAC AGAGGTCAGA CCCAGCCTGG 780
TAGTGGGATG GCAGCTATTG GGACTGGTGG TCCACGAGAT GGACAGACTC CTCTGGGGCC 840
AGTCCCACAT CCTCCTGTTC AGGGCTCCAT TGAGTGCACA CGACTTGGCC CAGAGCAGGC 900
ACCTAGGATT GCAGGTCAAA TGGGACTGCA GTGCCCAAGG ACAACAGAGG CAGGAAGGCT 960
TCCTGGAGGG AGGGGCCCTG GGGCCCTCAT TCTGGCTCAC 1000
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