Tag | Content |
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EnhancerAtlas ID | HS051-15973 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:128282330-128283750 |
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 | CTGGTCTCAA ACTCCTGACC TCAGGTGTTT GCCACCGTGC TCGGTCTACT TTTTAAAAAG 60 TAACTTAAAA ACACAAATGA ATGGAAAAAA AACTATTCTG AAAGTATCAG GAAAGTGTTT 120 TTTTGTTTTT GTTTTTGTTT TTGTTTTTTT TGAGACAGAG TCTTGCTCTG TCGCCCAGGC 180 TTGGAGTGCA GTGGTGCAAC TTCCGCTCAC TGCAACCTCT GCCTCCCGGG CTCAGGGCTC 240 AAAGGATCCT CCCACTTCAG CCTCCTGAGT AACTGGGACT ACAGGTGTAT GCCACCACAC 300 TCGGCTAATT TTTGCATTTT TTTGTAGAGA CGAAGTAGGG GGGTGGGGTA GGGGCGTAGG 360 GGGGTGGGGT ACGGGCATGG GGGGTGGGGG TGGTGTTGGT CTCACTATGT TGCCCAGGCT 420 GGTCTCGAAC TCCTGGGCTC AAGCCATCGG CCGCCTACGC CTCCCAAAGT GCTGGGATTA 480 CAGGCATAAT CCACCGCACC TGGCTTAGGA AAGTGTTTTT AAGCAGTGCA TGCCTGGAAA 540 ACGCTTTGCA GTCATTAGAA TTCACTGTCC TACGTAAGGA AAAGCAATGA ACTCAAAACA 600 GTAAAGGGCT TAACGCTTAA ACAATTATTT AAGCACTCAA GTTTTCTTTT TAATTTTCAA 660 TTTTTGTGGG TACATAGAGG GTGTATTTAT TTATGGTGTA TTTAAGAACT TTTGTAACAG 720 AACGCCCCAA CAGGACTAGC ACACAAAGGG AAAGCAAATG CGACGTGTTT CCCACACCAG 780 GTTCTGCCTC ACTTATCCTT AATCTCAGGT GCCAAGCACC GTGCCAGCAG AGTGGGCCCC 840 AGTAACAGCT TACAGAATAA ACAAACAGTA AAGAAAGGAG ACCAAACTTC GGTGAGGAGG 900 AAGAGGAACG ATCTCAAGGT GGAGGAAAGG CACAAAAACC ACCAGTAAGT GCCAGAAGCG 960 CATTCCTTAC TCTATGCATG CAACTGAAAC ATGGGTCCTG CACTTACGTC CGGTGTTGCA 1020 AGCAAGATTA AACCACTCCT AACTAGCAGT GAAAAGTCTA GGAAGGATCC CCCGCCCCAA 1080 CGCCCCTTGG ATTCTCCAAC TACTCAACTA CTGAAAACTC TCTTAACAGA AGACACCTCT 1140 CCTTCCCTGC ACACAATAGG AGCTTAACAT ATGAAAGTGA CTTCCCAATT TCAGCAAAAA 1200 CCTTCGCCGA TTCAGAAGAA AGCTTTCCCA CCAGAATCCC CTCTCCAACG TTCTAGCTTC 1260 GACGCTTGCA GCTGGTCAGA GGGCTCTTGC CCTCCTCGGG CCGGGTCGCG GGAGGGAAGG 1320 TTTCGGGGGG CCTCCTTGCC CCCACCCGCG GGGTGCCAGG CCAAGCCCCG CCGAGTAACT 1380 GCTCCGCCTC CCAGCCCGGT CCCCCAGGTC CCTGCCCCAC 1420
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