| Tag | Content |
|---|
EnhancerAtlas ID | HS145-09146 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr16:50752880-50753730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:50752883-50752901 | GGAAGGAAGGAAGGTTGA | + | 7.45 | | FOSL2 | MA0478.1 | chr16:50753529-50753540 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr16:50753529-50753540 | CTGAGTCACCC | - | 6.02 | | ZNF263 | MA0528.1 | chr16:50753340-50753361 | CCCTCCCTCTCTCCTTCCTTT | - | 6.72 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26957 | chr16:50752012-50754846 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I050718 | chr16 | 50752783 | 50754228 |
|
Enhancer Sequence | GAGGGAAGGA AGGAAGGTTG AGACTGGGCA CCTTGGACTT CAGTGCAGTC CTAAGACATC 60
TTGGCAAGGC TGATGAGGAG TTCTTGAACC AAATTCACCA GGCAGGGGAG CCTGATGTCT 120
CAGGCAGGGG CTGGCAAGTG CAGATGCGAG GATGTTAGAT TTTGGAGCAC AGCAGCTGGG 180
GCCCTTGGCT ACCTCCAAGG AGCTGAGGCT GGAGACCTGA AAGGCGAGTT CTCCTAGCTG 240
CCACACCCCT TCTCCAAGGA TACAATAATA TCTGCCTTAT AGGATTGTTG TGAGCTGAGT 300
GGCTTGACGT TCCTTGAAAG AATGAAAGCG TATAGTTATC CCAGGAAGCC TAGGGTTGCA 360
GGTGAGAGCT CTGGGGCTTC TCCGAAGCTC TCCGAGGTGT CTGGATTCAG TTGCAGCAGG 420
AGCCTTCCTT GCTGGGATCT TCCCCCACCC CTAGCCTTGG CCCTCCCTCT CTCCTTCCTT 480
TCTGGAAGGC TCAGTGGGCC CCACCCCTCC CTCCAGCCAC CTGGACCTGC CCAGCGCTCT 540
TGTGCAACAG GTAAAGCCTA CCTGTAGCAA CAACAGATCT GGGAAGGCTG CAGAGGGCAC 600
GATGGGGTCT GGATCGAGGG CGGCTGAGAC CAGAGGGAAA GGTGTGACCC TGAGTCACCC 660
TCGCTGTCCC GGGGAAACCA CCTCCCAGGA CAGCTGCCTA CTGTGGCTCC TGCCTGGAAT 720
TGTCACACTG CTGTGCAAAC AGCGTCCCGC TGCCCCTTTC CCTTTGCTGG GGGAAAATGA 780
AGTTGTGGGA GCCGCTGAGT AAACTAGACC TAGCAGCGAG GGCACCTGAT GTGGCTGCTG 840
CCTCCCGGGC 850
|
