| Tag | Content |
|---|
EnhancerAtlas ID | HS121-06921 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr11:64974290-64975520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr11:64975040-64975050 | GGGGCGGGGC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 64974492 | 64974582 | | chr11 | 64974956 | 64975106 |
| Enhancer Sequence | GTGCGTGGTC CCACCCCACC AGGCCCCGTC CTCCTCTCTT CCTCACCCCT GGGTGTGTGA 60
TGGGGACCCA GGTGTCCTGT CCCCTGAGTT CCTGCTAACA GGGAAGATCC CCTCCTGGTG 120
GAAGCCATAG GAGTAGTGCT AATCCCTCAT CCGCCCAGCA CTTTACAGTT TGCAGAGGAC 180
CTGTGATACT AATGGCACAG GCCCTGAGCT CTCACCCGGT GGCGGGTTTG TGCTGAGCAC 240
TTCACCTGTG TTACCTCATT TCCTCCCCAC ATCAACCCTG TCCGGGTCTT GTTACCATAC 300
CTCCTCTGAA TGGGAAATTC AGGTTCACAG AGGTTAGGGA ACTTGCCTGA GGCCATACAG 360
TAGGGATCCA AACTCTTGCC TTTTTTTTTT TTTTTTTTTT GAGAGAGTCT CACTCTGTCA 420
CCCAGGCTGG AGTGCAATGG CGTGATCTCG GCTCACTGCA ACCTCCGTCT CCTGGGTTCA 480
GGTGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCGCACG TTACCACACC 540
TGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTTGCC ATTTTGGTCA GGCTGGTTTC 600
AAACTCCTGA CTTCAAGTGA TCCACCCACC TCGGCCTCAC AAAGTGCTAG GATTACAGGT 660
GTGAGCCACC GCACCTGGCC CAAACTCTTG CCTTTTACTC ACTGAGCTGA ACAGCATCCC 720
CTTCATTTAG GTCACATGAG TGCTGGATAT GGGGCGGGGC AGGGCAGGGC AGGAACGAGA 780
TTCCCTTTTC AGATTAGAAA AGTGAGACTC AAGCCGGGCT CAGTGGCTCA CGCCTGTAAT 840
CCTAGCACTT TGGGAGGTTG AGGCGGGCGG ATAACCTGAG GTCGGGAGTT TGAGACCAGC 900
CTGGCCAACA TGGCAAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCC GGGCATGGTG 960
GTGGGCACCT TTAATCCCAG CTACTCAGGA GGCTGAGGCA GGGAGAATGG CTTGAGCCCG 1020
GGAGGCGGAG GTTGCAGTGA GCTGAGATCA CGCCACTGTA CTCCAGCCTG GGTGACAGAG 1080
TGAAACTCCA TCTCAAAAAG AAAAGAAAAG AAAAGTGAGG CTCAGAGAAG CGAAGTGACT 1140
TGTAGCAGAT ATGTGACCTC AGCCCTCCCT CCAGCTGCCT CCACACGGGC AGGGCCGGGG 1200
CCTCTCTTAC CTGCTTTCTC CCCTTCTCGG 1230
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