Tag | Content |
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EnhancerAtlas ID | HS108-02887 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:151728720-151730190 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr1:151728950-151728964 | AGGAAATGAGTCAT | + | 7.28 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATATGGCTCT GGGGAACAAA GGGTGGGTGT AGGAGCAGCC CGCATTATCA TCACTCCCAG 60 TGACCCAATT GAAGAAACTG TGCCTTCTAT CCCAACTCTG GTCTCTAAGG GTTTAGAAGT 120 CCTGGTTCCC AGAAGGGGAA TATTTGCACC AGTGAACACA CTGAATCTCA CTAAACTTTA 180 AGCTATGGCA GGCACTAGAT TACTCCAAAT CACTACCAAG AAACAAGGCA AGGAAATGAG 240 TCATTATCAG GAGGTGGGGC TGCTATTACA CAGTGGGGAC AGGGAAGAAT ATATCTGGCA 300 CCCAGATCAT CCACTTGAGT ATGTTTCTCC TTGCCCAATT TTGATGATAA ATGAACAAGT 360 GCAGTCATAG TCTGAGAAGG GCATGATGGC CAGGTACCTC ATCTGGTAAC CCACGTGAAC 420 CAGAGGTACA ACCCCCTCAA GGGGGTTGGG GAAAGATCAA CAATAGGTAG TAGAGAAGGG 480 AGGTGAATGC CAGTTGCAAA CTCAAGCTAC AGCAGCAGAG GCTGTGGCCT GTTCCAGACC 540 TTCCTCTTTT AAGTTTCCCC AGAAAGAGAT CCATCAGAAT CCTGAAGAAA CCATTCCAGA 600 ACTAATGAAA CAAATCAGTC TGAGCAGTGC AAAGGGTGGA CTGCAGTGTT GACTGTGGTG 660 TGCTGCCCAT ATTTTCCCCT TGAGGACTGA AGCTGCTAAG AATGCTGACA GCTGTCACCT 720 GTGCCTCATC CAGGGACCGC CTTTGGCTGA AGTTAGCCAC CTCACTCATG ATCATACCCC 780 TTTCCTGGTC AAGTGGGGAG ATAAGGTCCA GCCCACTTAC CCTACTGGGG CATCCTGCAG 840 AGCCATCCTA GTTTGAGCTC CTGATTGACT GAGGCGTTTG TTAAGACTGC ATCAGCTCAA 900 TTTCTCCCTC TACCCAATTC TACTGCCTTT ACTCCCCAAT AGGTGTTGAT GCAGATAACT 960 CCTCCCAATA AACTTCCTGC ATGTGAATCT CCAACACAGA GTGTTTTTGC CAAGAACTCA 1020 ACCTATGGCA GGTATTTAAA TGCTTTTTAA GGTTAGCTGT GTGAAATGTG TGCTCGTTGC 1080 TCAATTTCAG AGAGTTTCGT GATGGTCATG TTGAGAGATG CTGTGTGTGT TTAATTAGCC 1140 TACCATTTCA AGGACAATAG GAATGGGGAT CATTGAAATG GCAAATTTCA GTGGGCTTGG 1200 GGCTCATGCC GAGGCTGCAG GTCCTCCCCA AACCTCAGGA GCGTGTCCAG GATGGCAGAA 1260 CTCTGTGCTT CAGTTTGGGG GTTAATTCTG GGTGTCCCCA ACTCACTAGG GATTAACTGG 1320 GGTACAGAAG TGTATGCATC TACTTCAATC TAGATTAGCG CTTCCTAAAT ACTGGGGTCT 1380 CTGCAAGTTA ATGGAGGCTC AAACCTTTCA GGAAGTTCTG TTAAATCCAA GACTGAGTGT 1440 ACCTACCAAA AGCAGTCAAC CATCTTTCAA 1470
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