Tag | Content |
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EnhancerAtlas ID | HS113-37880 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:88131860-88132720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr9:88132328-88132339 | GGGTGACTCAG | + | 6.02 | FOXF2 | MA0030.1 | chr9:88132177-88132191 | ATTGTTTACCTGTG | - | 6.13 | JUNB | MA0490.1 | chr9:88132328-88132339 | GGGTGACTCAG | + | 6.02 | SPI1 | MA0080.4 | chr9:88132415-88132429 | AGAAAGGGGAAGTA | + | 6.59 | SPIC | MA0687.1 | chr9:88132415-88132429 | AGAAAGGGGAAGTA | + | 7.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_08307 | chr9:88130954-88132439 | Brain_Inferior_Temporal_Lobe |
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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 |
GH09I085516 | chr9 | 88130955 | 88132439 |
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Enhancer Sequence | CTCAAAGTCC ATGTCCTCTG GGAAACTTCT CCTGGTCCCC CACAGCGATG CTCACAGTTA 60 GTTGTTGGAG CACATTCTGC ATTCTGCTTT GTTCTCATAG CTGGGGGTGA GCCTGCCTGC 120 CTCCCAGCCA GACTGTCAGC TCCATGAGGG CAAAATGCAA CTCGGCACAT GCTCCTTTGC 180 CTGTGTGCTG TGTGTTCCCC TCTTCATGGG GCCCTCAGCA TGTCCTGCAT TGCTGTCTTA 240 CACCTCCAGC CCCCACTAGC CCCTTGATTC ACAGAGGAAA GAGAAACATT TGGTTCTAAT 300 ATTCCCTCCA CCTCTAAATT GTTTACCTGT GCCAGCTCTC GCCTCCTGTT TTGAGTGTGA 360 AAACCCAATA AGGGAGGTAG ATGGAGGTGT GGATTCCAGA TTGGCCAGTT TGTGTTTTAA 420 AAGCACACTC CCTGGAGGAG GCAACAAGGG AGGCAGGAGG CCCAGGCAGG GTGACTCAGG 480 CATATTAGTG GGTTGTCCAG AACAAGGTGT GTACCACATA GGAATGCAGG GCAGATGTGA 540 AAGCATCTAG TTTACAGAAA GGGGAAGTAT GGTTAATACA GTAGATGCTG GCCAGGTGCA 600 GTGGCTCACG CCTGTAATCC TAGCACTTTG GGAGGCCAAG GCGGGCAGAT CACCTGAAGT 660 CAGGAGTTCG AGACCAGCCT GGCCAACATG GTAAAACCAT GTCTGTGCTA AAAATACAAA 720 AATTAGCCGG GTGTGGTGGT GCACGCCTGT AGTACCGGCT ACTCAGGAAG CTGAGGCAGA 780 AGAATCACTC GAACCTGGGA GGCGGAGGTT GCAGTGAGCC GAGGTCATGC CGCTGCACTC 840 CAGCCTGGGG GACAGAGCGA 860
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