Tag | Content |
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EnhancerAtlas ID | HS064-00267 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:26856480-26857590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr1:26856530-26856540 | GGGGCGGGGC | - | 6.02 | NR2F1 | MA0017.2 | chr1:26856935-26856948 | CTCTTGACCCCTG | - | 6.04 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_05151 | chr1:26856168-26859913 | Brain_Cingulate_Gyrus | SE_06153 | chr1:26855244-26859852 | Brain_Hippocampus_Middle | SE_07004 | chr1:26855813-26859752 | Brain_Hippocampus_Middle_150 | SE_08385 | chr1:26856301-26859925 | Brain_Inferior_Temporal_Lobe | SE_23590 | chr1:26855659-26859611 | Colon_Crypt_1 | SE_24086 | chr1:26855638-26859463 | Colon_Crypt_2 | SE_32436 | chr1:26855678-26859550 | Gastric | SE_50663 | chr1:26855642-26859665 | Sigmoid_Colon | SE_52690 | chr1:26855673-26859562 | Small_Intestine | SE_60264 | chr1:26855575-26871102 | Ly4 |
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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 | GAGCGGGGCG GGGGACGGGC GCCCGCGGCC GGCGAGCCCG GATCCTCACA GGGGCGGGGC 60 GGCCCGAAGC GCCGCTGCAG TCCGGCGGGC GCCCGCGAGG GCGCGAGTGC CCTCCGATCT 120 CTTGCCCACT GTCCGGCTCC ACCCCCCTAT GCCCGGGTGT GCGTGTGCGA GGGACAGTTC 180 CGCCAAGCGC CGACTACCTC CCCGCCATAG CCAGGAGAGG GGATCCTATG GGGCGCTGAG 240 ATCTGGTCGC CTTCACCCCA CACCTAGGAC CCGTCCCGGC ATCTGTCCAG AGCTGTCGGA 300 GCTTCCTCCA TTAATGCAGA CGGGGAGATC TTCAGTGCCA GATGTCTGGG ATTCTACCAG 360 AGACAGGGGT TATGGGACCC CCACTTCTCC CAGGGCCCTC CGCCAAGAGC TCCCTGCTTC 420 TGGCTTCACC GCTGCTGAGC CTAGAAGGAT TGCTCCTCTT GACCCCTGGC GGATGCGGAG 480 TGTGGGATGG CACCACCCGT CTGGGGCTGG AACTCCTGGT TTTCTTTGCC CTGAGGCTAG 540 GGCCAGAGGA CACCTGTGTG CCCTACCCCA GGCTGTGGAG ACGAGAGTGG GGAAGAGCCC 600 TTAGACCTTG TGAAGATGAT TCCTGGCAGG GCGTGGGGGG ACCTTGGTGC CTGCCTCCCT 660 TCTTATGCCC CTTCCGGTAG GAAGGGCTGG GCCCTTGGGG AGTTTGGCTT CTGCCAGCCC 720 AGACTCCCCA GACAACCCAG CTCCTTCTCT CTCAGAAGCA GCTCCTGACC TCCCTTGAGG 780 GCTCTGTGGC TCCAGTCCCT AAGCGTGCAG AAGGCCACCT CTTCCTGTGC CTTTTGACCC 840 CAGGGTCAAG GTCAAGCCCC TGAATGAGCT GGTGGAAAAC TTCCTCCTTA ACCTCTTGCT 900 GGGAAGGAAG CAGGTGATAT TCTCCTTCCC AGGTGGTTGT TGGGGGTATG CAGGGAGGGA 960 ATGGAGACCT CATTTGAGCC CAGGAGCTGA GATGACTTTC TCCCAGCTTG GGCCTGGAGC 1020 CCCTGTCTCA GTCCCCTCCT CTGCCCTCTC TTACCTAGGG CAGCCACCAA GTGTCCTGCC 1080 TCTCAGGACC ACAGGCTTAG ATCAGGGTGA 1110
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