| Tag | Content |
|---|
EnhancerAtlas ID | HS082-37658 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr9:131959990-131961840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:131960857-131960875 | CTCTCCTTCCTTCTTCCC | - | 6.37 | | POU6F1 | MA0628.1 | chr9:131961720-131961730 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr9:131961720-131961730 | ATTAATTAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr9:131961105-131961126 | GGAGGATGAAGTGGAGGGAAA | + | 7.2 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53874 | chr9:131959911-131961757 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 131960013 | 131960156 | | chr9 | 131960252 | 131961661 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129197 | chr9 | 131959950 | 131961627 |
|
Enhancer Sequence | TGGCCTCCCA AAGTGCTGGG ATTACAGTTA TGAGCCACTA TGTATGGCCC AGTCCAGCTT 60
TTGTATTGGT TTACATGAGG CTTTTAGTTT GGATCTTTAT TCAATGCCTC TTCTGTGGAT 120
GAGATGGTGT GGGGTACAGA GGCAGGGGTG CTAAGACCAG CCCCTCCTGC AGGGAGAAGG 180
CCACGATCCT CCCTGACTCT TGTGGGGGCT TCCGTAATGC CCAGTACTGA GTCCCCTACC 240
CTGGGACCTG TGCTCTGCCT CTGGAATGGA AGCCACTCTG TAACCCCTAA AACCAGAGAA 300
ATTGGCAGCT GCTCCCTTGG CTGAGAACAT CGCTGACTCC AAGTGCCCCA GTGCTCTCCA 360
CTCATCATTT CACAGACGAC CCTGAGGGAG GCAGGGCCAG TGCGGCCTCA TTCCACAGAC 420
GAGGAAACAG TCTCGGCCAC TTGGCCAAGG TCCCAGAGCT TGTAAGGAGC AGATCTGGGA 480
TTTGAACCCA GGTCTGTTCA ATGCCAGAGT AACTGCCCTC TGTCCGGGCT GGCTGACACC 540
ACCCGTCATT TATTAGGCAG CAAATGGTTA TCCCGTCCTC TGGGCTTAGG GCTTATGGCT 600
GTGTTTGCGG GGTGGGGATG GAGTGGGAGG CGGGAAACAT TCCTAGTGGT GGGAAACCAG 660
ATGTGGGTGC AGGGAGAGAC GCTGGGAGAG GTGCCAGGTG TCAGGGGCCA CGCTGTGACA 720
TCTCCTCCTG GTGGAGGGTT CCAGCCCAGG GCAGGGGACG GAAGCTTCGG TGGCCCCTAC 780
GCTGAGCCTG GCATCTCTCG GGTCTCCTAG TGCTTAGAGC TGACACGGGG ATCAGTGCTT 840
GGCTGGCGCT TGCCAGAGGC AGTGTTTCTC TCCTTCCTTC TTCCCTTTTT TTCTGAGACA 900
GTGATCTTGG CTGTGGCGCC GAATCCGCTC TATGGGAAAA ACTTGTTTTT GTCGGTAAAC 960
TCGAGCGTTA TGACTCAGAA GACACCCAGG GAGCAGCCTC GTGGTGTCAA GGGGCCGCTC 1020
TGCTAATGAG CTAATGCTTA GGAAGTGCTT TGAAGACGAA AAATTCCACA CGAGGGTTGA 1080
GGGTGTGTGC TGTTATTTGG GGGAGAGGGT GAATAGGAGG ATGAAGTGGA GGGAAAGGGG 1140
CAAAATCTTG CTAAGGAACA GCCCCCCGAG ACCCTCGGGC TGCGCGGCAA GGCTGGCTTT 1200
GCGTGTTGCT GATGCAGGCG TCTGTCTGGG CAGAGGCACC AGCTGCCCCT TTGTTCAGAA 1260
CAAGGCAGAT CTGAACTGGG TGGGACACGC GGCTTTGATT TAGTTTTTCT TCCGGGGGAG 1320
GGGGCGGGCT GGGGTGGGAA GGGATGGGAC TTGGGTGACT CCTGTCGTCT AGCCTGAGAT 1380
CTTCCAGTCT GGAAGCAGCT GCTGTCATTC ATTCATTCAA CAAACACATC GACCTGCGCC 1440
AGGCATGGGC CATGGAGCAG GAAACGAAGA TAGTCCCTGT CCTCTTGAAG TTTATGGCCT 1500
GGAGGGGGAG ATGACATCTA ACAGATGAAG ACGTCAACCA CCTTGCAGTT AGAATTGTGA 1560
AAGGGTGGCG GCAGAGAGAC ACCTAAAGTC ATGGGTGCGG GAACCACAGA TGTCCCAGCC 1620
CAGGTCTGGG AGTGCCAGGA AGGCTTTCCC AGGAGGAACA GCTCAAAGGA AAGAGTGGGG 1680
GTTTCCAGCT CCCAGGCAGA GAGACAGGAC ACATCAGCAG AGAGATTGGC ATTAATTAAT 1740
ACACTGAATA AATGGCCGGG CCTGGTAGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC 1800
CAAGGCGGGT GGGTCACCTG GGGTCAGGAC TTTGAGACCA GCCTGGCCAA 1850
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