| Tag | Content |
|---|
EnhancerAtlas ID | HS003-19937 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr17:44331120-44331910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:44331362-44331381 | CGGCCAGCAGAGGGCGCTG | + | 8.57 | | ZNF263 | MA0528.1 | chr17:44331131-44331152 | GGAGGGGGAGGGGAGGGGGAG | + | 6.01 | | ZNF263 | MA0528.1 | chr17:44331124-44331145 | GGGAGAGGGAGGGGGAGGGGA | + | 6.37 | | ZNF263 | MA0528.1 | chr17:44331145-44331166 | GGGGGAGAGGGAGAGGGAGAG | + | 6.95 | | ZNF263 | MA0528.1 | chr17:44331134-44331155 | GGGGGAGGGGAGGGGGAGAGG | + | 7.17 | | ZNF263 | MA0528.1 | chr17:44331139-44331160 | AGGGGAGGGGGAGAGGGAGAG | + | 7.2 | | ZNF263 | MA0528.1 | chr17:44331122-44331143 | GAGGGAGAGGGAGGGGGAGGG | + | 7.42 | | ZNF263 | MA0528.1 | chr17:44331128-44331149 | GAGGGAGGGGGAGGGGAGGGG | + | 7.64 |
|
| | 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 |
| GH17I046253 | chr17 | 44330999 | 44331718 |
|
Enhancer Sequence | GAGAGGGAGA GGGAGGGGGA GGGGAGGGGG AGAGGGAGAG GGAGAGGTGC ATTTTCTTAT 60
AAACCCAATT TCCTCTTTAG TGCAACTCTA CCATTTGAAA GGAACCTTTC TATTGTAATT 120
TACAAGCTGT GAATAACCGC TATGTAATTC TTTCCAAGGA TTAATAAACT GAGAGAGGAT 180
TTGAACCAAC AGAGGTAGGG GAAGATTAGA AGGGGGATGC AAGTGGCCAC AGATCTTAGA 240
GGCGGCCAGC AGAGGGCGCT GCTCCAAGGT GAAGGTCGCA CCCTGAGAGG CCATCCTTTT 300
TTGTAGGACC AGACTGGGGT GTAAGGACAG TGCCTCATCC TCACAACGAC AGACCCGTGT 360
TCTGGGTGTG GATTTGCCTC CCTTGCCTGC GGGACTTCTG CTAGCACTGC CGTTCCTAGA 420
CTTAGACCAT GCTAGAATGA GTCCAGGAAC CGAGGAGAGG AGATGGGAGT GGCTCCTCCC 480
ACTGTGGCCC CTAATAATTC ACATGAAGAA TTTTTGCTTT CCTTGCCAGG GACCCGGGAC 540
TCAGTGGGTC CAGAGGTCCT AGTGCCAAAG GAAGAAATGT GTAGATCAGG AAATACTATT 600
ATGGTTTTAT TCAACTGGAA GCCGAGGCTG GCCATTTATT GTATTTATTT ATTTATTTAT 660
CTATCTATTT ATTTATTTAT TTAGAGACAG AATCTCACTC TTGTTTCCCA GGCTCCCAGG 720
CTCAAGAGAT CCTCCTACCT TAGCCTCCTG AGTAGCTGGT ACTACAGTCG CATGCCACCT 780
TGCCCAGCTA 790
|
