Tag | Content |
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EnhancerAtlas ID | HS093-18099 | Organism | Homo sapiens | Tissue/cell | HL-60 | Coordinate | chr2:171824300-171825960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:171824835-171824845 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:171824835-171824845 | GGCACGTGCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAACACTAAT CTCTAGGGAG ATTGAGGGAC TTTTTTTTTT TTTTTTTTTT TTGGAAACAG 60 GGTCTCGTTC TGTCACCCTG GCTGGAGTGC AGTGGCTTGA TCTTGGCTCA CTGCAGCCTT 120 GGCCTCCTGG GCTCAAGCGA TACCCCCACC TCAGCATTCC ACGTAGCTGG GACCACAGGT 180 GTGTGCCACC ATGACAGTGA GGGACTCGAC ACTCGACGAA TGGACACAGA CTCAGGCTAG 240 ATTGGCTCGT TGGATCTTCC CTGAGGTGGA AAATACTTCA TTATTTTCTG CTGTCTTCAG 300 AAAAGCCAGT TTCAGTCTTT AACAGTGGTA GATTTGGTAC CAGGTTCCAG AAACACGATG 360 TAAGAGAGAG TTTCCCTGAC AGTGGGCCAC TCTCCGTGGC CTTGTAGGGA GACAGACCAG 420 GGAGTCAGTC CTTAGGGCCA AGGCAGAAGG ATTGCTTGAG CCCAGGAGTT GAAGACCAGC 480 CTGGGCAACA TAGACCCTGT CTCTACAAAA AATTTAAAAA TTAGCTGGGC GTGGTGGCAC 540 GTGCCTGGAG TCCCAGCTAC TCAGGAGGCT GAGGTGGGAG GATCCCTTGA GCGCAGGAAG 600 TCAAGGCTGC AGTGAACTGT GAGGAAACCA TGCAAGGTTA GGAAAAGTCT TGAGTGTTTG 660 TGTGCATGGG GCTGGGGCCT GTGTGCTGGA CTAGGGAGTT TGAGCTTTGG CTTAAATACG 720 GCAGTCATGA AGGCTGGAGG GGCAGCACAG TGGGGGACCA GCTTCAGGAG GGACGCTCAC 780 CTGAACCCCC TTTGCTAAGA CTCTGAGTCT AGGATGACGA CTGTGTTACT CTGTTCTGAC 840 ACTGCTATAA AGAAATACCC AAGACTGGGT AATTTTATAA AGGAAAGAGG TTTAATTGAC 900 AGTTTCACGT GGCTGGGCAG GCCTCAGGAA ACTTACAATC ATGGCAGCAG AAGAGAAGCG 960 CAAGCAGGGG AAATGCCAGA GGCTTAGGAA ACCATCAGAT CTCGTGAGAA CTCACTCTCA 1020 CGAGAACAGC AGTGGGGAAA CCACCTCCAT ACTCCAATCA CTTCCCACCG GATCCCTTCC 1080 TCCACACGTG GGGATTATGG GAACTACAGG AAGAGATTTG GGTGGGACAC AGCCAAACCA 1140 TATCAGTGAC TTTACCTTTT CCCCTCTGAT TTTTGTTCCT GTTTTATTTT TAGTCCATTA 1200 CTAATTGTGC TTACCTGGGA GCAGCTTAAC TTAGCTCATT TTCTGAAAAT TCTGGAGACC 1260 TAGAAATGGC CTTGTGGCCT CTTCCTCACC TGAAAGGCAC CTACTAAAGC TCAAAGATGG 1320 CTCTGCCTTG GATGTCCAAA ATTTCTGCTT TTGACTATAG TGAAGATGAG ACTGGTGAGC 1380 TGCTGGAGCT ACGGTAGTGA CATGGAAGCC CTGATCCCAC CTTTAAGGAA CCTGTGGTTT 1440 AGGCGGGAAC ATGAGGCAAC TTCATGCAAA CTGCAGCAAG TGAAGAGTCT CAGCTGAGCA 1500 GAGACCTGGA GAGTCTGGGT GAAGGGAACA TTCTCTGGCA CCTGAAGAAG GCTTAGCCAG 1560 ACCTACATTT TAGCAGGTGG AGAAGGAGTT AAAAAAATCC AAGCAGGAGC CCTAAGGGAG 1620 CTCACAGTAG GAAAGCCATG GGTGTTAAAG CCTCCAGCAG 1660
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