Tag | Content |
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EnhancerAtlas ID | HS105-82704 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:116384960-116385930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr9:116385369-116385380 | GGCCAATCAGA | + | 6.02 | NFYB | MA0502.1 | chr9:116385364-116385379 | ACCTGGGCCAATCAG | + | 6.93 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_01545 | chr9:116384980-116386578 | Aorta | SE_02292 | chr9:116381830-116386777 | Astrocytes | SE_29700 | chr9:116380789-116385875 | Fetal_Muscle | SE_37366 | chr9:116381946-116388389 | HSMMtube | SE_38013 | chr9:116380995-116386367 | HUVEC | SE_44306 | chr9:116381993-116386918 | NHDF-Ad | SE_45031 | chr9:116382269-116385987 | NHLF | SE_45799 | chr9:116381711-116388595 | Osteoblasts | SE_55765 | chr9:116381308-116390127 | u87 | SE_65476 | chr9:116385248-116386339 | Pancreatic_islets | SE_67932 | chr9:116381308-116390127 | u87 |
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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 |
GH09I113619 | chr9 | 116381352 | 116386641 |
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Enhancer Sequence | CACCACGTTA TCATGACTCC TTTGGATGAA AAACCAATAA CCAGTGTGTA TCAGGATTGT 60 CTGTAGTGTA AGAGTTCATA ATCAATGAAT GAGAGGACTC TCTGATGAGT CAGGGATGTG 120 GATTTTTGAC ATTTGTTTTG GCAGCTGAGA ATAAGGGGTA GTTTTTTTCT TTCTAATTTT 180 CACCCCAATA GCAGCTGCTT TCTGAGAGTT TTCTAGATAA ATGTGAAATG AGTGTAGATC 240 GATTTTTCCA TGTAACTAAT TTACATTCTG GGTGAACTCA TTTTGCTTCT GACTTAGAGG 300 TGCTTTCATT TCCTTCTCAT CTGCACCCTG TTCTTGGAGA AGCTGCTCCA CCCCTAGCCC 360 ATGATACATG ATGCATGACC CAGCCCACTG GGCCCCCTGA TGCCACCTGG GCCAATCAGA 420 TTTTCCAGTC AGGAAATTTG CAATTGAGAT TCAGAGCTGG AAAGAGTCAC CTGCTCTGAT 480 GGGAGCTGCA TTTGTGGACT GTGACTCAGA GGCTGAGGCC CCAGGGAGCC GACCCCATGG 540 GCCCTGGGCA AGCCCAGAGT GAATGTGGAA GCCGGGCTGT GGAGGTTCCC TGAGCAGACA 600 GTCCGGGTGT GTGTGCGTGT GTTTGTCTGT GTGTGTGCGC ACATGCTGGA GGATGGGGCA 660 GAACGTAGGG TCCCAAGCCC CTGAGGGAGG GGCTTGTCCT AATCAAGTCA CAGAAATCAG 720 GGCAGGGAGA GCATGAAAGA GTCTTGTTCC CCTCTCTGCA TTTGGGAGAT TCAGGCCCCG 780 GGGAGAGGAG AGACTGACCC ATGATCATCC AGAGGGGACT TGGTTAAGCT GGTCCTGAGC 840 TCTGCCATGC ATGTTCTGTT TTCCTACCCT GGCAGCTGGC TCAGAGCATG GATAGGCCTT 900 GTCTCTCTTT TCTTTCTTTC TGCCAAATTC TTTTCTGTTG GGAATCTGAA CAGCGGGTAG 960 ATGCAGTCAT 970
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