Tag | Content |
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EnhancerAtlas ID | HS105-74736 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:101016420-101017840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr7:101017022-101017037 | CTTTTCCTGAGAATC | + | 6.34 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68974 | chr7:101016134-101016944 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 101016768 | 101016820 | chr7 | 101016888 | 101017832 |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I101372 | chr7 | 101016135 | 101016944 | GH07I101373 | chr7 | 101017201 | 101017350 |
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Enhancer Sequence | GCAGAGGAAG GATAGTGGAA GGAGGGAGGC CAGTTAGGAG GTAGTTGATG GATGGAGCAG 60 GGGAGAAGGG AGTGCTCAGA GCTAGCAGGA CCTGGCCCCT TGGTGGATCA CGGATAGGCA 120 GAGACAGGCT ACAGGCCTGA GCTCCTGGCT GTCTCCAGTG CCTGGGGGAC ACCAAGGAGC 180 CTGCTGCTTT GCTTCTCAGA ACATTGCAAA TTTTTTGCAG CACTTTCTTG GTTTGCAATG 240 GCAGCAAAGC AGAGTTCAAA CATCTTGCAT TTTTGTGAAA TACTTTTATT TTTCCTGCAT 300 GGAGTTTTCA ACCCCAAATT TCAGCATCTC CTGGACTTGC ACGGATCAGG TGCTCAAGGA 360 AAGTTTGTTG AGTGAATGAA TGAACACATG AATGAATGAA CAAATACCTT GACCTTTCTC 420 CTTTGGGACA CCGAGGCAGT GCCTCTGCCT CAGTGCACGT TTGCAGTTCT GAGGGATCCT 480 GGAGCGAGGT CCCTTTCTCT GCACAGGCCA GCTCCTGAAG CTGCTTTTAG GGGAACCATG 540 GAGACTCCAG CTTTAGAGGT CCCGCTTCTC CCTTTGAAGT GTGAGCACAT AGAGGAGGGA 600 GACTTTTCCT GAGAATCACA CAGAATGGCT TTGATGTTAA TATCAGTGAG ACCTTGTCCT 660 CAAGCTCCAG GATTTTCTGA ATCTTCCCTC TCTTCATCTC ACTCCCCTCT TCCCCCAGCT 720 CATCTGTTAT TTTAAAATCC ATTCCCAGAG AAACAATTCC TATGGCAATA AGAGCACTCC 780 TCCAGGCTTC TCTTGGCTCG AACTCGTGTG ACACTTCATT GCCACTTCCA GAGTGTGTGA 840 GCTGGACCCG GACCAATTCA GCCTGGGGCA GGGGAAAAGA GCAACAATAA CTAACTGTTA 900 GAGGATTTTC GGGAATGTTA GCACAAAGTG CTCCGGGAAT TCTGCAGACA ATCCTACGGA 960 AACATACACA TGCCGTGCTG TTCTGCCCTC CGAGTTGTCA GGGGTCCCTG GCCTTCCCAG 1020 CCTGGCCTTG TCTCTACCTG CCTCCCAGAA ACCAGGGTCT AGAGCTTCTC TTCGGAGTCC 1080 TGTAACAGAC TACCCTGAAA CAAGCTGGAC TGAGTCCAGG TTAATTCTGA AATACTGGAG 1140 GAGAGCGGTG TGCGTTCTGG CCCCCTGCAT CTCCTTGTTT GCCCCACCCC TAACTACCTC 1200 CAGAGTGATC TATGTAAAGC AGGAGTCCCC AACCCTGAGG TCACAGACAA GTACCGGTTC 1260 AAGACCAGTT CAAGGAACCG GGCCGCACAG CAGGAGGTGA GTGATAGGCG AAAAAGCCTG 1320 AAGCTTCATC TCTACAGCTG CTGCCCTCGC TCGCATTACT GCCTTAGCTC TGCCTCCTGT 1380 CAGACCAGCA GCGGCAGTAG ATTTTCATAG GAGCTCCAGC 1420
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