Tag | Content |
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EnhancerAtlas ID | HS060-36394 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr9:140639900-140640500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr9:140640360-140640375 | ATTGCTGAGTCATGC | - | 8.55 | Nfe2l2 | MA0150.2 | chr9:140640362-140640377 | TGCTGAGTCATGCCT | - | 7.3 | SREBF2 | MA0596.1 | chr9:140639950-140639960 | ATCACCCCAT | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_10754 | chr9:140638878-140640811 | CD19_Primary | SE_11232 | chr9:140638468-140641129 | CD20 | SE_32711 | chr9:140638399-140641999 | GM12878 | SE_59172 | chr9:140631350-140657613 | Ly3 | SE_62965 | chr9:140561512-140658488 | 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 |
GH09I137744 | chr9 | 140638883 | 140641502 |
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Enhancer Sequence | AGTTTTTTCT CCTCTTATAT GAAGAAGCAT GAGGAAGAAA ACACAGCATC ATCACCCCAT 60 TGTCCTGGTG GCTCTGGCAC TCTGAAACAG TCACTACAGG AACTTCCTTA GACGTGCCCA 120 GCACAGCCCA GCCCTCCCCG AAGGACAGGC AGCCCTGACT GCACCGTGGG GAAGCAGCTA 180 CCCCAGCAGC TGCCGCGGTC TCTGCACACA CGTGTCTGTC GCTCCAGTGC ACTGTCTGTT 240 CAGCTGTGTT ACGCTCTTTC TGTCAAGTTA CAAGGGGTAT TCAGTGTCAC AGTTTTGCTG 300 AGTATGCCGG AGGCTCATAA GTGCTGTCTG CATTTACAGT GTAGCACTTT GATGTCACCA 360 GGCCACCTCT GACTGTATCC TTCCACCTGC AGAGACCTGA GGGGTGTGGT TTCCTCACCT 420 TCCCCAGCAG GGCTGCCTTC TTGGAGTCCA GCAGCTCTTC ATTGCTGAGT CATGCCTGGG 480 GCTGAGCAGC CAGCCACCAG TGTTTGTTCC TCTGTAAGCC GCTTGCTAAA TAGCCCCTGC 540 TCATTTTTCT TCTGGATTTT GCATCTTTTG AATGTAGTCT GACGATCTTT TTTGTCAACG 600
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