Tag | Content |
---|
EnhancerAtlas ID | HS133-03608 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:223252270-223253440 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR1 | MA0162.3 | chr1:223253123-223253137 | TACGCCCACGCAGG | + | 6.24 | EGR2 | MA0472.2 | chr1:223253124-223253135 | ACGCCCACGCA | + | 6.62 | EGR3 | MA0732.1 | chr1:223253122-223253137 | TTACGCCCACGCAGG | + | 6.13 | EGR4 | MA0733.1 | chr1:223253122-223253138 | TTACGCCCACGCAGGA | + | 6.03 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTCTGGCTG CTGGAACGTT TATTCCTCCA TCAGGGCTTG GGCCATTCCA GGCTGGGGAG 60 AAGAGGCCAG AGGGAGGAGG GAGGCCCCCA GCCAGGTTCC GGCTTGGGCA GTGCAGCCAG 120 CAGAGGGGCT TAGGAGCAGC AGGCAGTGGA GTCCTGAGCA GAAGCAGGAG GGTTGCAGGG 180 CTGTGCTGGC ACCAGCCGTG GTACAACTGG GGCATGGATG ATGACTGAAG ATGGTCAGGT 240 AGAGGAGAGT TGAAGCTTCT ACCCTACATG TGTGCTCACT GTTCAGGAGA CTCATCAGCG 300 CTGCTTTACA GTGTGGTCGC TGGCTTTTCC CAAGAGAAAG AGGAAACTGC CAGGACTGCT 360 AAAGGCTGGG CCCAGGACTG CTGCTCCTTC TATGGCTCGA CACAGGGGGA AGGGGGACAG 420 CCTCGCTTCT TGCTGGGGCT GATCACAGGG GAAGAGGGGT CCAAGGCCAC CATTGGAGAC 480 CACGCATTCT ACGTGAGGGC CACGGGTCCC CCTGTGTCTG CCTTTCCACG TGGGGAGGGG 540 TACATAGCAG CTGTGAACCT CTCATCTGCT GCCCCAGGCT TTTGGATCCT GTCAATGCAC 600 AGACTCTGAC AGACTCAAAC ATCTGCCTTC CAGCCTCGGC CATGTACTCT GGTGACTTCC 660 CCAGAATGAG TGTGGCAGGT CGCCTTGATC CAAGTAGCTG CCAACTCACC CTTGCCCTCT 720 TAAACAGCCC CTTTGTGGAC AGTGGTCAGT GACAGAGACA TGGGTGACCT GCTGAGTGGG 780 AGGGGAAGGC TCCTCTCTGG AGGTTCAGAG GTGGAATTCA GACCCGCAGG CCAAAGTCTC 840 AGAAGGCAGA TTTTACGCCC ACGCAGGAGT GAATAATAAA CTCTTTAATA CTGGAGTGGT 900 CTGATTTCCA AAAGGGGGTG CCCTGTCCCT AGAAGTGTTC ACACAGAGGC CGGATCATCC 960 CTGCCGGGAG AATGAGAATG AATTCCTACA CTCGTGGAGA GGCTGGACTC TTTAAACTTC 1020 CAAGATTCCT CACGCTTTTA ATCATCCTTC ATTCTAATTA TCCAGACCCT ATTTGGTGAC 1080 AATTATCATT TGCAAGTCCC AGCAATCCTC ATTTTGGGGG CCAATCCCTA GTTGCTTGTG 1140 TAAGTAAGCA TTGTTGAGAA AAGGGTCCAA 1170
|