| Tag | Content |
|---|
EnhancerAtlas ID | HS002-01156 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:223252300-223253380 |
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 | TCAGGGCTTG GGCCATTCCA GGCTGGGGAG AAGAGGCCAG AGGGAGGAGG GAGGCCCCCA 60
GCCAGGTTCC GGCTTGGGCA GTGCAGCCAG CAGAGGGGCT TAGGAGCAGC AGGCAGTGGA 120
GTCCTGAGCA GAAGCAGGAG GGTTGCAGGG CTGTGCTGGC ACCAGCCGTG GTACAACTGG 180
GGCATGGATG ATGACTGAAG ATGGTCAGGT AGAGGAGAGT TGAAGCTTCT ACCCTACATG 240
TGTGCTCACT GTTCAGGAGA CTCATCAGCG CTGCTTTACA GTGTGGTCGC TGGCTTTTCC 300
CAAGAGAAAG AGGAAACTGC CAGGACTGCT AAAGGCTGGG CCCAGGACTG CTGCTCCTTC 360
TATGGCTCGA CACAGGGGGA AGGGGGACAG CCTCGCTTCT TGCTGGGGCT GATCACAGGG 420
GAAGAGGGGT CCAAGGCCAC CATTGGAGAC CACGCATTCT ACGTGAGGGC CACGGGTCCC 480
CCTGTGTCTG CCTTTCCACG TGGGGAGGGG TACATAGCAG CTGTGAACCT CTCATCTGCT 540
GCCCCAGGCT TTTGGATCCT GTCAATGCAC AGACTCTGAC AGACTCAAAC ATCTGCCTTC 600
CAGCCTCGGC CATGTACTCT GGTGACTTCC CCAGAATGAG TGTGGCAGGT CGCCTTGATC 660
CAAGTAGCTG CCAACTCACC CTTGCCCTCT TAAACAGCCC CTTTGTGGAC AGTGGTCAGT 720
GACAGAGACA TGGGTGACCT GCTGAGTGGG AGGGGAAGGC TCCTCTCTGG AGGTTCAGAG 780
GTGGAATTCA GACCCGCAGG CCAAAGTCTC AGAAGGCAGA TTTTACGCCC ACGCAGGAGT 840
GAATAATAAA CTCTTTAATA CTGGAGTGGT CTGATTTCCA AAAGGGGGTG CCCTGTCCCT 900
AGAAGTGTTC ACACAGAGGC CGGATCATCC CTGCCGGGAG AATGAGAATG AATTCCTACA 960
CTCGTGGAGA GGCTGGACTC TTTAAACTTC CAAGATTCCT CACGCTTTTA ATCATCCTTC 1020
ATTCTAATTA TCCAGACCCT ATTTGGTGAC AATTATCATT TGCAAGTCCC AGCAATCCTC 1080
|
