Tag | Content |
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EnhancerAtlas ID | HS059-44875 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr8:27190300-27191370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZBTB18 | MA0698.1 | chr8:27191341-27191354 | CATCCAGATGTGA | + | 6.07 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_08208 | chr8:27191183-27193111 | Brain_Inferior_Temporal_Lobe | SE_09156 | chr8:27181374-27208460 | CD14 | SE_10868 | chr8:27181046-27285079 | CD20 | SE_18325 | chr8:27186895-27191430 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20066 | chr8:27187970-27193004 | CD56 | SE_22414 | chr8:27187957-27191473 | CD8_primiary | SE_27921 | chr8:27189260-27194488 | Fetal_Intestine | SE_28623 | chr8:27189169-27194496 | Fetal_Intestine_Large | SE_50221 | chr8:27189287-27193915 | Sigmoid_Colon | SE_52630 | chr8:27189370-27193798 | Small_Intestine | SE_53591 | chr8:27189274-27193699 | Spleen | SE_62276 | chr8:27181124-27271753 | Tonsil |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH08I027330 | chr8 | 27188095 | 27194337 |
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Enhancer Sequence | GTTGGCCAGG CTGGTGTTGA ACACCTGGGC TCAAGCAATT CTGCTTCGGC CTCCCAGAGT 60 GTTGGGATCA CAGGCATGAA CCACCACTTC TTCCCCCTAA TTTGAGGAAT TATATCTGTC 120 CTCACAAAGT TTATAGTATG GTAGGGGAGG CAATACATGA AGATAAAGAA CTGTAAGATA 180 TTTATTTAAC TCTAAGTTAC TTAAAGGTAA ATAATGTGCC ATAAAAGAGG CACGAAGTGC 240 TATGAGATTG CAGGGCAGAG ATTCCTTCTG GCTATGGACT CTGGGAATGC TTCCTGGAGG 300 AGACGGCATT TGGCAAAGCT CTGAAAGGAT AGACAGGATA CACTGTGGGA ACTTGAGATG 360 GTGGCTGTAG TCAAAGAAGA GTATAAATAA CAGCAGAGAG ATGGAGAGGT GTGGTTTGAG 420 TGACTCATTT TGGGTGGAAC CAAGAGTGGC AAAAGGCAAT CAGAGTTGGG GGTGGAACGG 480 AAGATAAGGC TTGGACAGGG AGGCCAATGT GTTTGGGAGT TATCCTGGAA GTCCCAGACA 540 GCCATGGGGC TTTATTCTGA AGGCAGTAGG AGCTGTTGAC CATGCTGACT TCGGTGGAGG 600 TGCGAGGGTC AGATTCTGGT GTGTAGAGTG GATGAGAGTG AAGAGAGCTT GAATTCGCAA 660 GGGAGCAGAT AAGAGAGTGT TGTAATATTT CAGGCCTCAC ACATCTGAAT AAATTGCGTA 720 ACTCAGATAC TTTGCGGTCC TGTGGAGCAT GCAGGCATCC CCTGGAGGCT TCTACTTTCT 780 CTGAGCTGAA ATTGGTTCTT TGATGAATTT GAGAGATATA TAACTTATGA GAACATCCAT 840 GAGAAACCCA CCATTCCTCT TCACCTCTGT CTTCCATATT CTTGATTCCC AGCCTGGCCG 900 CTTCCCCCTG GGCCTCCCCT CTGCTAGGAG TGTGTTAAAT GCCAAGCCTG TCTCAACCTC 960 TATCTGGCAG CACCTTGAAG TATCAAGTCA GGAATATGCA CTTAGATCCA CAGGCCCCTT 1020 CTCCATCATG TCTCCGGTGA CCATCCAGAT GTGATGATTC CCAGGACCCT 1070
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