| Tag | Content |
|---|
EnhancerAtlas ID | HS118-19329 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:96382150-96384060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr9:96383049-96383059 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr9:96383049-96383059 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr9:96383049-96383059 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_65512 | chr9:96381177-96383011 | Pancreatic_islets | | SE_65512 | chr9:96383148-96384654 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH09I093620 | chr9 | 96382663 | 96382790 | | GH09I093621 | chr9 | 96383149 | 96384654 |
|
Enhancer Sequence | GTGACATTTG TGCCCCTGGT GGCCTCTGAG GTCTGTGTGT GGCCAGGCAC CGCCTCTCTC 60
AGCTCCTGGG TTTTCTCCTG GTCTGGTCTG CCCTGAGTTT TTGGAGAAGC AGAAGCCCTG 120
CTTAGCACAG CCTTAGAAGG CGTCCCTGGG CTTCAGCTCA GCCAAATGCC CTGCTCTCCC 180
TCGGACTCTG CAGTCCTGGC TCACCTGACC ACAAGCAGCC TGTGACCTGC TCTTTCTGCA 240
GATGTGGGTG GGCTCCCGGG ACAGACCTGC AGGGCCCAGC CTGGGAGTGT ACAAGGCTAG 300
GTGGCCAGCG GCCTGCAGAG GGCTCCAGCT CCTGTTCCCA GGAGGGAGAG GCCCACCTTC 360
TGTCTTCTGA AAGGTCTGAG TCTGGGGCCC TGGTTCTGTG AGGACCGTCC TCACCCACTT 420
CCCCACATCT GGGTCCTCAT GGAGCCTCTG TCTGTGTCCT GGGATGCATC CCCACGCTGG 480
GGCAGGGGCA GCAGGTGAGG CACGAGGGCC TGTCTGCAGG ACATAGGTGG ACGAGTGGGC 540
CTGGCTGGGG GATCCTTTGT GAGCTCAGCT CCTGTGAGCC AGCACTGTCC CCATGGGCGA 600
CAACCTTTGA AGTCAGCAAG ATGTGGCTGC TTGCCTCTCA GGTGGCCCAC GATGGGCTTC 660
CTGCAGAGGG CAGAGTGGAC ACAGGCCACA AGCACGTGGA TATCTGGGAA TTGCCCACTC 720
TGCATTAGTG AGGGGTTGAG GTTGGTTTTT TGTTAATGAG AAGCTTGTGC TTGTTTTTGT 780
CTCTGAAATA ATGAAGTCAT CTGCTAACAT GGCCTTGGGA TGCTGTAACT GTTTTGGTGT 840
TACCTAGTCT CCTTCAGATT CTCAGTATCT TATGCTCCTG GCTTTAGTGT GAGGAAAATA 900
TTTTCCATTT TTCTGTAGTT ATTATTCTCC TCTTATTTTT CGTTTTGCCA ATTTTCTGAA 960
TAATTTCTTA GGGGGCATTT AGAAAGCCCT AATTCTGGTA CAATAAAATA AATGCCCAGT 1020
GTCGGCAAAC AGTCTCTTCT GTGAGAACAG GATGGCCCCT AATGGAGCTC ACTGTGCTGG 1080
AGCTTGCACA ATCGAAGCCC TGGATCCTCG TTAGGTGCTG TCTCCTTGGC ATATAGCCAC 1140
AGCTAGTGGC AGAGCCAGGC TGAATGCCCT GAGACTTAGT TTCACCTGCC AAGTGGCCAC 1200
TGTCGGGGTT GGTGGCACAG GCAGCAGGGG TTGGAGCAGC AATGCAGATG TAGGGTCGGT 1260
GCTAGCAGGG GATCTGGCCT GGATCCCTGT GGAGGGTCTA CTTCCTTCAG CCTTGGAGGG 1320
GCAGGAGGGG CAGCCCAGTG GTCACCCCCC ACAACCCTGG TGGGCGGGCC CTGGATGCAG 1380
CCCCTGCCTC TGGCCCAGGC ACCTAGGTGG TGAGGGGGTG CTGAGGCCTT TGGTTCTCTG 1440
AGCTTCTTTT GGGCGGCAGA AGGACCCTTC CACCATGACC ACCTCTCTTT TCTCTCAGTC 1500
TCTTGGGGTC TCCTGCACAA AGCAGTAAAT GACTGACCAA GGCAGCTGTC CTGGCCAAGG 1560
TGAGGCCTTT CACCTGTGCC ACCCAGTTCA TCCTCCCAGC AGATGGCCCA GGGGTGGGTG 1620
GTGCTGGAAG GAGGAAGCCC ACAAGGGGCC CCTCCTTGTG CAAGTGGATT GGCTGTGCCA 1680
GGGCAGAGCG TCCTAAAGTG GACACTGGCC CAGAGCCTGG AGCCACACAG GTGGGCACGT 1740
TATGGAGGGC GGGGCCAGGT GTGAGGACTG GATCCCCACC TGACCTTTGT GCCTCTGAGT 1800
CCTTGTGCTG GCCGTGCACG TTCTTGTGAC CCCTGAGCCT CGGCCTTCCC CCCTGTAAAG 1860
TAGGCTTGTG CTGTCTGCCC CCAGGATCCA GGACCCCGTG CCAATATCCA 1910
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