Tag | Content |
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EnhancerAtlas ID | HS098-31436 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:128282770-128283750 |
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 | AAGCCATCGG CCGCCTACGC CTCCCAAAGT GCTGGGATTA CAGGCATAAT CCACCGCACC 60 TGGCTTAGGA AAGTGTTTTT AAGCAGTGCA TGCCTGGAAA ACGCTTTGCA GTCATTAGAA 120 TTCACTGTCC TACGTAAGGA AAAGCAATGA ACTCAAAACA GTAAAGGGCT TAACGCTTAA 180 ACAATTATTT AAGCACTCAA GTTTTCTTTT TAATTTTCAA TTTTTGTGGG TACATAGAGG 240 GTGTATTTAT TTATGGTGTA TTTAAGAACT TTTGTAACAG AACGCCCCAA CAGGACTAGC 300 ACACAAAGGG AAAGCAAATG CGACGTGTTT CCCACACCAG GTTCTGCCTC ACTTATCCTT 360 AATCTCAGGT GCCAAGCACC GTGCCAGCAG AGTGGGCCCC AGTAACAGCT TACAGAATAA 420 ACAAACAGTA AAGAAAGGAG ACCAAACTTC GGTGAGGAGG AAGAGGAACG ATCTCAAGGT 480 GGAGGAAAGG CACAAAAACC ACCAGTAAGT GCCAGAAGCG CATTCCTTAC TCTATGCATG 540 CAACTGAAAC ATGGGTCCTG CACTTACGTC CGGTGTTGCA AGCAAGATTA AACCACTCCT 600 AACTAGCAGT GAAAAGTCTA GGAAGGATCC CCCGCCCCAA CGCCCCTTGG ATTCTCCAAC 660 TACTCAACTA CTGAAAACTC TCTTAACAGA AGACACCTCT CCTTCCCTGC ACACAATAGG 720 AGCTTAACAT ATGAAAGTGA CTTCCCAATT TCAGCAAAAA CCTTCGCCGA TTCAGAAGAA 780 AGCTTTCCCA CCAGAATCCC CTCTCCAACG TTCTAGCTTC GACGCTTGCA GCTGGTCAGA 840 GGGCTCTTGC CCTCCTCGGG CCGGGTCGCG GGAGGGAAGG TTTCGGGGGG CCTCCTTGCC 900 CCCACCCGCG GGGTGCCAGG CCAAGCCCCG CCGAGTAACT GCTCCGCCTC CCAGCCCGGT 960 CCCCCAGGTC CCTGCCCCAC 980
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