Tag | Content |
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EnhancerAtlas ID | HS107-15650 | Organism | Homo sapiens | Tissue/cell | Jurkat | Coordinate | chr5:935370-936780 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr5:936596-936610 | ATTCCCATGGGACT | - | 6.91 | EBF1 | MA0154.3 | chr5:936596-936610 | ATTCCCATGGGACT | + | 7.52 | HSF1 | MA0486.2 | chr5:936418-936431 | TTCTGGAATGTTC | + | 6.59 | ZNF263 | MA0528.1 | chr5:935898-935919 | GGTGGAGCAGGAGAGAGAGAG | + | 6.24 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCCACCAGA TACTCTAAAT CATCTCTCTC AAGTTGAAGT TCCACAGGTC TCTAGGGCAG 60 GGGCAAAATG CCACCAGTCT CTTTGCTAAA GCATAGCAAG AGTCACCTTT ACTCCAGTTC 120 CCAATAAGTT CCTAATCTTC ATCTGAGACC ACCTCAGCCT GGACTTCATT GTCAATATCA 180 CTATCGGCAT TTTGGTTGAA ACCATTCAAC AAGTCTAGGA AGTTCCAAAC TTTCCCACAT 240 CATCCTATTT CTTCTGAGTC CTCCAAACTG TTTCAACCTC TTCCCATGAC CCAATTCCAA 300 AGTTGTTTCC ACATTTTCAG GTATCTTTGT AGTAATGCCC CACTTTCCTG GTACCAATTT 360 TCTGTATTCA TCCATTCTCA CACTGCTATA AAGAACTACC TGAGACTGGG TAATTTATGA 420 AGAAAAGAGG TTTAATTCAC TCAGTTTCAC AGGCTTAACA GGAAGCATGG GTAGGAAGCC 480 TCAGGAAACT TACAATCATG GCAGAAGGGG AAGCAAGGTA CATCTTGTGG TGGAGCAGGA 540 GAGAGAGAGC GAAGGGGGAA GTGCTGCACA CACTTAAACC GTCAGATCTC GTGAGATCTC 600 ACTATGATGA GAACAGCAAG GGAAGTTGGC CCCTTGGATT CAATCACCTC CCACCAGGCC 660 CCTCCTCCAA CTTGACATGA GATTTAGGGG TGACACAAAT CCAAACCATA TCACTAATCT 720 TCCCTTGTGG CGAGATGAGC AGCTCAGTGT TTGCACAGCC TGAGGAATGA GTGAATTGCT 780 GCAACTTAAA CTTCCAGCAG GCAGATGACA AGCTGTCCAT TCGACACAGT CAAAGGCTTG 840 GTCTTACGCT GCGTGTGTGA CTACAAGCAG ACCCTCTCTC GCCTGCGTGA GGAAGTGGAG 900 TTGATACCTA TTACATGGCT CAACACTTTA GTCATCGGGT CCTCAGGAAG TTGGAAGCCT 960 CTAAGCCCAG AGGCAGCCTG GACCCTTCCT CACAGATGCT TGGTGCTGGC AGTCCCACAC 1020 TGTCCCCCAC GGTGGCAAGC GGTGGTGTTT CTGGAATGTT CCACTTCACC CTCGTTCCTG 1080 TGTGTTCTCC TGCCCATGGT CTGTTGTCAC GAGGCCTGTG CCCTGACGCT GGATCTGCCT 1140 GTCTCCGGCC GCTGCTGGGT CCTGCTCTGC ACCTTCATGA GAAGCCATCT AGGAAAGTTT 1200 CTTCTTGTTT CTCCCGACTG GGGTTCATTC CCATGGGACT GGGGAACTGG GACTTTGCCC 1260 CGCTTTAAAG TTCTCCCTCT GGCTTCCTCC GTGGGCTATA GCCCTGACCC CACCCCAGCA 1320 CGGAGAGAGC CAGTCGGCAT CCTGGCTGCC CACTCAAGCT GGTGCCGTCA CAGGGAGAGG 1380 CTGGGTTGGG AATCATGACG TCTTTGGATA 1410
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