| Tag | Content |
|---|
EnhancerAtlas ID | HS052-19191 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:47242150-47243280 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr19:47242343-47242357 | CTGCCACGTCACCC | + | 6.73 | | REST | MA0138.2 | chr19:47242861-47242882 | GCCCCTGACCATGGTCCAGAA | - | 6.46 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGGCAGACA GGAGGCAAAG GGAGATAATG GGGCTCAGGC TCAATGCCGG TGTGTCTATC 60
ACTCACCCAG GTATAGTGCC AGCCCACAGT CACCCCACAG TAATGGGCAG CAGCCACTTC 120
CTCAGGCACA AAGATCCCAA GCCAGGGTTC AGGGAGCACT GAGAGGACAG GATGGATCTG 180
TTTCCAGGGC CCCCTGCCAC GTCACCCACA ACGAGGGCCG AAGGGGAGCC CTTAACCCCT 240
GAGATAACAA TGGGGCCAGC CTGGGCCTCA CCTGGTGGCT GCCTTTGGGG GGAAGTCGGG 300
TCAGGGATGG CAGTGGAGAG GAGGGTGGGC ATTCACCGCC CTGGACTACC CCTGACGCCC 360
TCTGGCAGGT GCTGTCCCTA AGGCTGCTGG TGGAGGTGGC GTCCCACTAT TCTTACCAGA 420
GCATCTGTCT CTGGGAGGCG TGGGAAGCTA CTTCTGGAGC TTAGGGACAA GAGTGGGTGG 480
CTCGGCTCGG CTCCTGCTCC AATAGAAAAG CTTTACAAGC CAAGCCCGCT GTGGGGACCA 540
GCCGTCCCAC TGCATTCCGC CCAGGGTGTG AGAGAAATGT GCCACAGACA CGACCCCGGG 600
TTCCTGCCAA GCACTTCACA CCGTCTGCTG GCTTGAGCTG CCCCGTCTGC TCCAGTCTGT 660
CAACAGGTCA TTTGGAGACA CTGGGCCCAC TGCCTTCCAG GCAGGATCCT GGCCCCTGAC 720
CATGGTCCAG AAGCTCTTCT GCCAAAGCCC TGGCCCAAGG CTCATCTCTG GCTTCTCCCC 780
AAGCACCCCA CCGTTCCAGC CCAGAACAGC CAGAGCCCAG GCCCAACTTA GACACTTACT 840
CGCTACATGA TCTTACGCAG GTCATCAGCC TTCTCTGAGC CTCCATTTGC CCCTCTAGAA 900
AATGAGAGTC ACAAGAGTGC CCTCCCCTCA TGTGCTAGGT TCTGCTCAGT CAAGGCCTGG 960
CACAGAATAA AGGCTAACAA ATGCCAGCTT CTACTTCTTT CATCATTTTT ATTCTCCCTG 1020
TCCATTGTTC GCAACTTCGA AATGGGCCCA GTTCCTTACG GGAGGTAGGA TCCCTTGGAG 1080
ACCCCAGATC AACTAGAAAT GTCTGTGGAT TGGCCAGGCA CAGTGGCTCA 1130
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