| Tag | Content |
|---|
EnhancerAtlas ID | HS120-02834 | Organism | Homo sapiens | Tissue/cell | LNCaP-abl | Coordinate | chr17:53315460-53316620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr17:53315795-53315806 | TGCGCATGCGC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH17I055237 | chr17 | 53314453 | 53316761 |
| Enhancer Sequence | CCCATTTGCA GGATAAATTC TGAGTTGCGG AACTAGTGAT TTACAGGGCA GAGGTGCAGT 60
CTTTGTCTTA ATTTCTGAAT TCACGAATGT TGAATGTGAT GAATTCGTGG GAAGCCCCGC 120
AGGGAGCCTA AGCAGCTCTC CAGAGGCTGT GGTTGTCACG GATGATGATT GCGGGACCCG 180
CAGACTGAGT CTCCAAGCGC TCCGCCCCGC CGCGCCCCTC TCCGCGGGTC CCACCGCGGA 240
CCCGCCCCTG CGCGCCCCGG GCCAGGAGCC CCTAGCTGCA GGACCAGGCA CGTGCGATTC 300
CACGTGAGCC TCCCGGCCGG AGCGCAGATG GGAAGTGCGC ATGCGCCTAC CGCCTGGAAA 360
GTAGGTCAGA CTCCTCCTCT CACGTGACCT GCTCCCCTTA GCTACCCTCG GCGCCTCCCC 420
GCCGGGGCGC AGCCGGGATG CGCTCGGCAG CCAACGTGAC GGGGCTGGGC GCGGGCGGCT 480
CCGCGAGCGC CCAGCGCCCG CGAGGATTTG CCGGTTCTCC TCACACCCGA GCGCTCCGCT 540
CAGAAGTCGG GCGGGCAAAA GGGAGCGCCT CGGGAAGTAT CTGGGAGCCG GGCTGGAAAT 600
GAATGGGGCC CGGAAGCGAG CTCAAATCGC TGACACCTGG CACCGGGCTG CGTCCACTTT 660
CATGCTTCCT AAGGCAGTTC TGCCTGCAAG AAGGGAACGC GCATCGCCTT TCAGTAGATC 720
ACACCGATCG TTTGCACGTT TGCATTCTCA ATTTCTGCAC TATATAGGGC AACTCAGACA 780
TGAAAACAAT CTTTGTAAGA AGAAGTGGAA TGCTAATGGT TCCTGGAGTT TTGCAGGAAT 840
ATTCCACCGG CCCCATTTCT AATCTCCCAC TCACTCCCTC CCCAAAGACA CTCCTACTAG 900
AAAGCTTATC GGTAGATTTC TCACCTTCCA CAAGAGACTT CAGGGGCGCT GCTGCTGCTG 960
CTGCTGCTGC TGCTGCTGCT GGAGGCTGGA GGGGGTTGGG AGCAGGGAAC GAAGGCAGGT 1020
CTGAATTAGC TGAAGCTAAA TTCTATATAT CAGAAATAAT TTTATTTATT GCCCCATTGC 1080
TTTCTGATTT TTAACTTGTT GCACAAATGA CAGACTCTGC CTCAGTGAGT TGCAATCCAG 1140
TGGAGGGCAC TAACAGGCAA 1160
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