Tag | Content |
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EnhancerAtlas ID | HS105-45330 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:128282460-128283750 |
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 | RREB1 | MA0073.1 | chr2:128282710-128282730 | GGGGTGGGGGTGGTGTTGGT | - | 6.57 |
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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 | GTTTTTGTTT TTGTTTTTTT TGAGACAGAG TCTTGCTCTG TCGCCCAGGC TTGGAGTGCA 60 GTGGTGCAAC TTCCGCTCAC TGCAACCTCT GCCTCCCGGG CTCAGGGCTC AAAGGATCCT 120 CCCACTTCAG CCTCCTGAGT AACTGGGACT ACAGGTGTAT GCCACCACAC TCGGCTAATT 180 TTTGCATTTT TTTGTAGAGA CGAAGTAGGG GGGTGGGGTA GGGGCGTAGG GGGGTGGGGT 240 ACGGGCATGG GGGGTGGGGG TGGTGTTGGT CTCACTATGT TGCCCAGGCT GGTCTCGAAC 300 TCCTGGGCTC AAGCCATCGG CCGCCTACGC CTCCCAAAGT GCTGGGATTA CAGGCATAAT 360 CCACCGCACC TGGCTTAGGA AAGTGTTTTT AAGCAGTGCA TGCCTGGAAA ACGCTTTGCA 420 GTCATTAGAA TTCACTGTCC TACGTAAGGA AAAGCAATGA ACTCAAAACA GTAAAGGGCT 480 TAACGCTTAA ACAATTATTT AAGCACTCAA GTTTTCTTTT TAATTTTCAA TTTTTGTGGG 540 TACATAGAGG GTGTATTTAT TTATGGTGTA TTTAAGAACT TTTGTAACAG AACGCCCCAA 600 CAGGACTAGC ACACAAAGGG AAAGCAAATG CGACGTGTTT CCCACACCAG GTTCTGCCTC 660 ACTTATCCTT AATCTCAGGT GCCAAGCACC GTGCCAGCAG AGTGGGCCCC AGTAACAGCT 720 TACAGAATAA ACAAACAGTA AAGAAAGGAG ACCAAACTTC GGTGAGGAGG AAGAGGAACG 780 ATCTCAAGGT GGAGGAAAGG CACAAAAACC ACCAGTAAGT GCCAGAAGCG CATTCCTTAC 840 TCTATGCATG CAACTGAAAC ATGGGTCCTG CACTTACGTC CGGTGTTGCA AGCAAGATTA 900 AACCACTCCT AACTAGCAGT GAAAAGTCTA GGAAGGATCC CCCGCCCCAA CGCCCCTTGG 960 ATTCTCCAAC TACTCAACTA CTGAAAACTC TCTTAACAGA AGACACCTCT CCTTCCCTGC 1020 ACACAATAGG AGCTTAACAT ATGAAAGTGA CTTCCCAATT TCAGCAAAAA CCTTCGCCGA 1080 TTCAGAAGAA AGCTTTCCCA CCAGAATCCC CTCTCCAACG TTCTAGCTTC GACGCTTGCA 1140 GCTGGTCAGA GGGCTCTTGC CCTCCTCGGG CCGGGTCGCG GGAGGGAAGG TTTCGGGGGG 1200 CCTCCTTGCC CCCACCCGCG GGGTGCCAGG CCAAGCCCCG CCGAGTAACT GCTCCGCCTC 1260 CCAGCCCGGT CCCCCAGGTC CCTGCCCCAC 1290
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