| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01747 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:223252250-223253790 | 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 | CTCGTTCAGA TGTTTCTCCA GCTCTGGCTG CTGGAACGTT TATTCCTCCA TCAGGGCTTG 60
GGCCATTCCA GGCTGGGGAG AAGAGGCCAG AGGGAGGAGG GAGGCCCCCA GCCAGGTTCC 120
GGCTTGGGCA GTGCAGCCAG CAGAGGGGCT TAGGAGCAGC AGGCAGTGGA GTCCTGAGCA 180
GAAGCAGGAG GGTTGCAGGG CTGTGCTGGC ACCAGCCGTG GTACAACTGG GGCATGGATG 240
ATGACTGAAG ATGGTCAGGT AGAGGAGAGT TGAAGCTTCT ACCCTACATG TGTGCTCACT 300
GTTCAGGAGA CTCATCAGCG CTGCTTTACA GTGTGGTCGC TGGCTTTTCC CAAGAGAAAG 360
AGGAAACTGC CAGGACTGCT AAAGGCTGGG CCCAGGACTG CTGCTCCTTC TATGGCTCGA 420
CACAGGGGGA AGGGGGACAG CCTCGCTTCT TGCTGGGGCT GATCACAGGG GAAGAGGGGT 480
CCAAGGCCAC CATTGGAGAC CACGCATTCT ACGTGAGGGC CACGGGTCCC CCTGTGTCTG 540
CCTTTCCACG TGGGGAGGGG TACATAGCAG CTGTGAACCT CTCATCTGCT GCCCCAGGCT 600
TTTGGATCCT GTCAATGCAC AGACTCTGAC AGACTCAAAC ATCTGCCTTC CAGCCTCGGC 660
CATGTACTCT GGTGACTTCC CCAGAATGAG TGTGGCAGGT CGCCTTGATC CAAGTAGCTG 720
CCAACTCACC CTTGCCCTCT TAAACAGCCC CTTTGTGGAC AGTGGTCAGT GACAGAGACA 780
TGGGTGACCT GCTGAGTGGG AGGGGAAGGC TCCTCTCTGG AGGTTCAGAG GTGGAATTCA 840
GACCCGCAGG CCAAAGTCTC AGAAGGCAGA TTTTACGCCC ACGCAGGAGT GAATAATAAA 900
CTCTTTAATA CTGGAGTGGT CTGATTTCCA AAAGGGGGTG CCCTGTCCCT AGAAGTGTTC 960
ACACAGAGGC CGGATCATCC CTGCCGGGAG AATGAGAATG AATTCCTACA CTCGTGGAGA 1020
GGCTGGACTC TTTAAACTTC CAAGATTCCT CACGCTTTTA ATCATCCTTC ATTCTAATTA 1080
TCCAGACCCT ATTTGGTGAC AATTATCATT TGCAAGTCCC AGCAATCCTC ATTTTGGGGG 1140
CCAATCCCTA GTTGCTTGTG TAAGTAAGCA TTGTTGAGAA AAGGGTCCAA CAGCTGGAAT 1200
CCAGGAAGGC CCTACCTACC TAGGCACCAT GTTAATGCCC AGCTAGTCAG TTGGGTCCAA 1260
GCGGCTTTGA GTATTTCTAT TTTAATATAA CTGCATGAAA TTCGCGCACC CGGGAAAGAG 1320
CTCGTGCGGG GTCACTGAGC ACCTTCTTTT CTTGGCCCTG AGGTTGGGCT GGGGGTGGAA 1380
AGGACCCTCA GCTCAGAGCC CTCCGTGAGG CCCCCAGCAT CTACTGCATC ACAGATTGGA 1440
CTGTCCCCAG CCACAGGACA GGGCTCAGGC CTCCCAGTTC TCCAAGAAGC GCATTCCCTG 1500
GGGTTGGCCC ACAGGACCGG GCTTCTCCGT TCACCTTTTC 1540
|
| |
|
|
|
