Tag | Content |
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EnhancerAtlas ID | HS187-13906 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:128282780-128283750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr2:128282960-128282971 | AAGCACTCAAG | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_19088 | chr2:128282403-128286609 | CD4p_CD25-_Il17-_PMAstim_Th | SE_27871 | chr2:128282507-128286757 | Fetal_Intestine | SE_28747 | chr2:128282686-128286988 | Fetal_Intestine_Large |
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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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Enhancer Sequence | CCGCCTACGC CTCCCAAAGT GCTGGGATTA CAGGCATAAT CCACCGCACC TGGCTTAGGA 60 AAGTGTTTTT AAGCAGTGCA TGCCTGGAAA ACGCTTTGCA GTCATTAGAA TTCACTGTCC 120 TACGTAAGGA AAAGCAATGA ACTCAAAACA GTAAAGGGCT TAACGCTTAA ACAATTATTT 180 AAGCACTCAA GTTTTCTTTT TAATTTTCAA TTTTTGTGGG TACATAGAGG GTGTATTTAT 240 TTATGGTGTA TTTAAGAACT TTTGTAACAG AACGCCCCAA CAGGACTAGC ACACAAAGGG 300 AAAGCAAATG CGACGTGTTT CCCACACCAG GTTCTGCCTC ACTTATCCTT AATCTCAGGT 360 GCCAAGCACC GTGCCAGCAG AGTGGGCCCC AGTAACAGCT TACAGAATAA ACAAACAGTA 420 AAGAAAGGAG ACCAAACTTC GGTGAGGAGG AAGAGGAACG ATCTCAAGGT GGAGGAAAGG 480 CACAAAAACC ACCAGTAAGT GCCAGAAGCG CATTCCTTAC TCTATGCATG CAACTGAAAC 540 ATGGGTCCTG CACTTACGTC CGGTGTTGCA AGCAAGATTA AACCACTCCT AACTAGCAGT 600 GAAAAGTCTA GGAAGGATCC CCCGCCCCAA CGCCCCTTGG ATTCTCCAAC TACTCAACTA 660 CTGAAAACTC TCTTAACAGA AGACACCTCT CCTTCCCTGC ACACAATAGG AGCTTAACAT 720 ATGAAAGTGA CTTCCCAATT TCAGCAAAAA CCTTCGCCGA TTCAGAAGAA AGCTTTCCCA 780 CCAGAATCCC CTCTCCAACG TTCTAGCTTC GACGCTTGCA GCTGGTCAGA GGGCTCTTGC 840 CCTCCTCGGG CCGGGTCGCG GGAGGGAAGG TTTCGGGGGG CCTCCTTGCC CCCACCCGCG 900 GGGTGCCAGG CCAAGCCCCG CCGAGTAACT GCTCCGCCTC CCAGCCCGGT CCCCCAGGTC 960 CCTGCCCCAC 970
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