Tag | Content |
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EnhancerAtlas ID | HS047-33908 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr9:34373000-34374210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:34373802-34373820 | GGAGAGGAGGGAGGAAGG | + | 6.15 | ZNF263 | MA0528.1 | chr9:34373799-34373820 | GGGGGAGAGGAGGGAGGAAGG | + | 7.26 | ZNF263 | MA0528.1 | chr9:34373804-34373825 | AGAGGAGGGAGGAAGGGAGAA | + | 7.48 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28440 | chr9:34373606-34378083 | Fetal_Intestine | SE_32207 | chr9:34373696-34377899 | Gastric |
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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 |
GH09I034372 | chr9 | 34372398 | 34373429 |
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Enhancer Sequence | TGCTCTGAAA GGAGGAGACA GAGATGGAAC TGAGCTATCT CATCCCATGA TATTTCCATT 60 TGCTGCCGCA AGCTAAGAGG AGGTGTATAC TTTGGGAAGA TGAATACTGG AACCTGAGGG 120 CTTGAAGAGT GGCAAAGGTG AGACCCTTAC CAGGACAATC TGTGCCTAAC CCACCCTTTC 180 TCATGGGACC TAATGCTTGC CCAAATTAGG ACTCTGTGAC TGGGGAGCGG CCCATGTGAC 240 TGGGAGATGG CACCCATCCT CATTTTCCTA GTGGAGAAAC AAACCCTGAG AGGGTCAGGA 300 AGCTTTCCAG GATCACAGGA TAAGCCAGGC CTCCCCAGAT CACACATGGG GCCGTTCGGG 360 CTGAAGAGAC GGGAAAGGAA CTAGAAAAGT CCTGCTCTCC TAGAGGTGTG GATGGTCAGG 420 GTGGGAGAGG GGGTATTGTC CAGCCAGCTC CTTGAGACTT TTTTTTTTGA AATGGAGTCT 480 CTCTCTGTCA CCCAGACTGG AGTGCAGTGG CATGATCTCA GCTCACTGCA ATCTCTGCCT 540 CTTGGGTTCA AGCGGGTCTC CTGCCTCAAC CTCCCGAGTA GCTGGGATTA AAGGCGCACA 600 CCACCACACC TAGCTAATTT TTGTATTTTT GGTAGAGACA GGGTTTCACC ATGTTGGTCA 660 GGCTGGCTTC GAACTCATGA CCTCAAGTGA TCCACCTGCC TCAGCCTCCA GAAGTGCTGG 720 CATTACAGGC GTGAGCCACC TCGCCCAGTC CCCCTTGAGA CTTTTAACAG GGCGGTAGGC 780 TAGCTTCCCT GTCCCCAGAG GGGGAGAGGA GGGAGGAAGG GAGAACAGCT CAGGGATGTG 840 TTTTTATCCT GAGTCAAAAG CCTGATGAAG TCTGGAGATT GAAGAAGACA CCCAAAGCCA 900 GACTTAGTCC CAGGGCCTGG TTTGGAGGGA GGTAGAGTTG GGTTCAGACA TTAGGGCCTG 960 GGGCAGGAGC CTGGCATGGG GGGCCAGTTG TTTCTCACAT CTGCTTCTCT TTGCCCTCAA 1020 ACTCACCCTG CTCTCAGCCA TCATCCATCA CCAAATCCAT TTCCATGCCT GCCTTCCTGC 1080 TTTGCTCCTG GCACCACATC TGTGGGCCAG CTACTTCCTC GCTCTGTTTC ACCCACTGTC 1140 CTGTTTCTGT CATAGTTTGG GCACTGTCAC TTCTCCCCTG TATTACCAAA CGCTTCCCCC 1200 AACAGGCCTC 1210
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