Tag | Content |
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EnhancerAtlas ID | HS105-83127 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:126097570-126098510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr9:126097783-126097798 | TGCCCTCTGCCCTCA | - | 6.14 | ZEB1 | MA0103.3 | chr9:126097777-126097788 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr9:126098171-126098192 | TCTTTCTCTCCCCACTCCCCC | - | 6.5 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_08129 | chr9:126097200-126099181 | Brain_Inferior_Temporal_Lobe | SE_10272 | chr9:126097554-126099554 | CD19_Primary | SE_11088 | chr9:126096409-126109430 | CD20 | SE_27373 | chr9:126096704-126099799 | Esophagus | SE_58675 | chr9:126066110-126112932 | Ly1 | SE_59949 | chr9:126072819-126109309 | Ly4 | SE_60622 | chr9:126083387-126112614 | DHL6 | SE_61709 | chr9:126066543-126112588 | Toledo | SE_62912 | chr9:126066502-126108695 | Tonsil | SE_68067 | chr9:126071237-126113711 | TC32 |
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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 |
GH09I123335 | chr9 | 126097350 | 126099393 |
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Enhancer Sequence | CTTATCAGAA GGCCCTCATG CCTACAGTTA GAGGAAGGGA CAGAACTTGC ATGCACACCA 60 GGCCACCTAA CGATGACACA CAAGATGAGC ATTGTCAACC CCATGTTATG GCTGAGGGAC 120 TCAGCCTCAG AGAAGTAAAT GAACTTGCCC GAGGTCATAG ATGAGAAATA GCAGAACTGG 180 GATTGGAGCC CAGGGTCTTT GCCTGGCCCC ACCTGCCCTC TGCCCTCACA GCCCTATTAC 240 TCCTTCCATG ATGGGGGTGG CAGACATCCC AGGCTGGGTC TCCAGAGCAG GCCCAAGTCT 300 GGGCCTCAGG GCAAGGTCAT CAGGAGGCCA AAGAGGGAAA TCTTTAAATG GTGTCAGGTT 360 CATTGCCTTT GTGGCAGAAG GAAGAAAAAA GAAGAGGCAC AGAAGCAAGG AAGATGGAGC 420 TGATTCCTGC TTAACTCACA CCCTCTCGTT TGGCTGAGTC AGCGATGCAG GGAGGCCTCC 480 CTGGCCTCAG CACAGAATCG CAGGAATCTG CAGATCTGCT GGAATTTCTC TGCACTGGCT 540 GGCACGGGAG GTGACGAGAG CAGAGGAAAA CGACTGCTGT TTTTATTCTC TGGGGCTGGT 600 TTCTTTCTCT CCCCACTCCC CCCCGGCTTC TTGCTCATGT CTTTGAAAGG CCACTTGTCT 660 CTGACTTGCA CAGCACTCAA CAGTCTAGAA AGCCCCTACA AAGAGCTCTT CGGTCCCCAA 720 AGTGATTTAT GATTTTGAAG TGCTTTTTGG ATTATGAAAG GCTAACCTAC AATAGCCTCC 780 TCACTGCGGC AACATTTACA AAGTGCTTTG CAAGTCACAC GGCATTTTAT AGTTTGCAAC 840 ATTCTTTGCA GCCAAAAGGT GCTTACCTCT CCAGAGGGGA CTTCAGAGTT TGCAAACCCT 900 GGTCACACCT CTTCCTTTAT TTAAACTGCA GTACAGCTCT 940
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