Tag | Content |
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EnhancerAtlas ID | HS176-02943 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:183573000-183573990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ATF3 | MA0605.2 | chr1:183573576-183573588 | GATGACGTCATG | - | 6.37 | ATF3 | MA0605.2 | chr1:183573576-183573588 | GATGACGTCATG | + | 6.44 | JDP2(var.2) | MA0656.1 | chr1:183573576-183573588 | GATGACGTCATG | + | 6.27 | JDP2(var.2) | MA0656.1 | chr1:183573576-183573588 | GATGACGTCATG | - | 6.74 | JUN | MA0488.1 | chr1:183573574-183573587 | ATGATGACGTCAT | + | 6.15 | SPIC | MA0687.1 | chr1:183573881-183573895 | TTCTTCCCCTTTCT | - | 6.03 | ZNF263 | MA0528.1 | chr1:183573032-183573053 | GAAGGAAGATGGGGGAGAGGT | + | 6.09 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09925 | chr1:183567023-183580226 | CD14 | SE_53951 | chr1:183572134-183575523 | Spleen | SE_59245 | chr1:183570687-183580261 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 183573151 | 183573904 | chr1 | 183573035 | 183573933 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I183602 | chr1 | 183571737 | 183579934 |
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Enhancer Sequence | TCCACTTCTG TCCGCTGGGA CGTAGAATGG TGGAAGGAAG ATGGGGGAGA GGTGTCCTGA 60 ATTCTAGAGA AGTGGTTTCT AGCAGAGCAA AGAAACATAC AAGAAGCTAT TGCAATATTT 120 CAGGCAAGAA ATAATGCTAA GGCAGCCACA GGAAGAGAGG ATGGATGTGG ATAAATGCCA 180 AATACAATGT GGCATTTCAC ATGGAGACAA AGGAGAGTGA CTGGGAGGCT GGTGACACCC 240 GTGACTGCCA CAGGAAATGG AGTGGTAACC TCATCCACCC CTACACTTTC ATACAAGTGA 300 CTCTCAAGGC ATGCTTCTGG CCATATTGTC TCCCGAGAGC AGAAATCTGA AGACAACTGA 360 TATGGCCTTT AATAAATGGG GACTGAACTT TGGGGAGGCC CTAATTAAAG ACAGCTGGAG 420 CCCTGGGGAA AAGGAGCCAG TGGAGACTGT GGGAAAATGT CAGAGAGGCA GGAGGAAGGT 480 GAGACCACTG CGGTCAGCCA CATCTGACTC AGCTCTTCAA GGAGGGAGGT GGACGGTGCG 540 GAGAGCTGCT GGAGGGGAGG GGAAGCTGAA GACCATGATG ACGTCATGGC CGAGCTGGGG 600 CAGTGGGCAG AGGAGGCGGA AGTCAGGTTG TGAAGAGCTG AGGAGATAGT GGGGGCTGAG 660 AGGATAGAAG GGCTGGATGC TCTCCCTGAA CTGTGAAAAG GAAGAAATCA TGCTGCCCAC 720 AGGTGGAGTA GCCCAGGAGA AGGGCAACCC TGGGTCTGCA GCCCCCGCCC CTCTGCCTCT 780 GTGTCTTCCT CACACTGGGC TCCCAAGCCT GTGTAGGCTT GAGTCTTTCT GAAACTTTGG 840 TCAGTCTGTG GTAACACCTT TCCCATGATG AAACATGTTT TTTCTTCCCC TTTCTGCATC 900 TTCATTAGTT GCCTTCCTCC TAAACAGAAC TCGGCAGCTA AATTAGGCCA AAACCCCAAC 960 TCATTTCCAA CAAAGTTCAC CAAATAAGCT 990
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