Tag | Content |
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EnhancerAtlas ID | HS018-13767 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:241974600-241976200 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr2:241975592-241975603 | GGGCGGGAAGA | + | 6.14 | KLF4 | MA0039.3 | chr2:241975281-241975292 | AGAGGGTGTGG | - | 6.02 | RREB1 | MA0073.1 | chr2:241975446-241975466 | ACGGGGTGGGTGGGGGGTGG | - | 6.25 | RREB1 | MA0073.1 | chr2:241975478-241975498 | GGGTGGGGGGTGGGGGGTGG | - | 7.47 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I241034 | chr2 | 241974300 | 241977304 |
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Enhancer Sequence | CCTCAGGGCC ACCCATGAGG CAGGTCCTCT TACCACCCAG GTCCTCATTT TTGCCAGCGG 60 GCTTGCTGCT TGGTGGGATT TGGTGACTGC TTGACAAACC CAAGCATCAC GTCTACAGGG 120 GAGTTCCAGG GGTCCTTCCA GCCCACAGTG CACAAACGGA CGGGGTGGGT GTCCCTCCCA 180 GGGGTGGGCA CGTGGTTTGT GGGAACAGCC AGGGCGGCAG CAGAGCCATA GATGGTAGCC 240 TTAGCCCTGC TGCTGTGCGG CCTTGGGAGC CAAGGAGCCT TCAGAAATCA CTGCTTACAC 300 TTGGGGCGAG GGCAAGCGAC TGATCCGCTC CACTGAGGGC GGCGCATCAC AAGCCCTGCC 360 AAGCCTGGGG CCGCAGTGAG GCTCGCACCG GGACCTGCCC CAGACTCGCC TCCCAGCCGC 420 GAGCATCTAG GCTACGAGAG GGGAGAGGGG CCGCATCTCC GCAACACTGA GTCCCCAGAG 480 AACACGACAG GGGTAGCAGA TGCGCGCGCA CCACTGTCGG GGCGGAGGCG GGGTGCAGGC 540 GCGCCATGGG GTGGGGGATG AGGGGTAGAG AGTGTGGGGG TGGGGGATGG GGTATGCAGG 600 TGCGCCACAG GGTTGGGGAT GAGGGGTAGA TGGTGTGGGG ATGGGGGGTG CAGGCGCGCC 660 ACAGGGTTGG GAGTGAGGGG TAGAGGGTGT GGGAGGTGGG GGCGTGCCAT GGGGTGGGGG 720 GTGCAGGCGT GCCACGGGGT GGAGGGGTGG GGGGTGCAGG TGTGCCACGG GGTTGGAGGT 780 GGGGCGTAGT AGGGGTGGGG GGCGGAGGCG CGTCACGGGG AGGGGAGTGG GGGGTGGAGG 840 TGCGTCACGG GGTGGGTGGG GGGTGGAGGT GCGTCACAGG GTGGGGGGTG GGGGGTGGAG 900 GCGCATCACG GGGTGGGGGT TGGGGAGTAG AGGCGCGCCA CGGGGTGGGG AGAGCACCGC 960 GCGCTCATGG GAAGAGGAAA GATGCAGTCG CAGGGCGGGA AGACCCATCT GAGGGCTGCA 1020 GGTGGTGCCG CGACGAAGGA GGCCCGAGGA GCCCGAGCTA CCCACACACT GGGGCACGAA 1080 CAGGCCCCCG CTTGCATCTG AGCTTAGGGA GTCCGGGCTC ACGGGGCGGG GAGCCCAGAG 1140 CGGCCGCCCA GCATCCGAGG GACACAGCCC TCCTGCAGCC CCCAGCCACA CCCCCTGCGT 1200 GGCCCGCCTT GTCCCAGAAA CGCTGACATG ACGGCTGAGT GCCAGCCTCG GGTTTTCCAC 1260 GCCAGGAACC CTGGAGGGGA GGCGGAGTGT GCCAGTTTTT AGACCTGTCC ACGGCAGCGC 1320 TGAGAGGGAT GGAGGGGACG GGGTGCTGGT GTGAGTCGCT TCAGGGAGTC CGCCCCACAC 1380 GAAGCCACCT CCCCAGAGGC CACGCCAACA GCACCGCCCC TGCTCCCCTG CTCCCCTGCT 1440 CCGACCTAAA GTGAAACCTG AAACCTGGCT GCTTTGCTGC GGTCACCCGG GCACCCAGAG 1500 GCCGACCTTT TGGGTCAGGG GAGGGAAGGG AGATGCGGAT GGGAGTGGCT CTCCTGCCGA 1560 GTCCGGAGGC AGCGGCTGAG GCTCCAGCCC CTCCCTATGT 1600
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