| Tag | Content |
|---|
EnhancerAtlas ID | HS158-41006 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr3:184209940-184210510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr3:184210031-184210042 | AGCCACACCCA | + | 6.14 | | ZNF263 | MA0528.1 | chr3:184210401-184210422 | AGGGGAGGACGGAGAGAGAGA | + | 6.32 | | ZNF263 | MA0528.1 | chr3:184210382-184210403 | AGAGGAGGAGAGAAGAGAGAG | + | 6.65 | | ZNF263 | MA0528.1 | chr3:184210385-184210406 | GGAGGAGAGAAGAGAGAGGGG | + | 6.82 | | ZNF263 | MA0528.1 | chr3:184210373-184210394 | GGGGGAGAGAGAGGAGGAGAG | + | 7.51 |
|
| | 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 |
| GH03I184492 | chr3 | 184209905 | 184210788 |
|
Enhancer Sequence | AAGTGAAAAT GAAGTCTCCC TCCCAGTCCC CACGCCCCCA GGTTCAGTCC GGGGCGCCTG 60
GACAGGTTGG CATTGGAAAG CGTGAGGAAG CAGCCACACC CAGAGCGCAC TGCGGCTATC 120
AGAGATGGGG TCTCCGGATC TGCGACTTCC ACGAGGCGCT CGCGAGGGGG AAGTTAGGAA 180
CTGGTTTCGC AAGGAAGGAT GCGGTTGGCA CACAGTGCGA GGAGAAAGGG GTTCTTCGGG 240
CTGAGCGCGG GCTCGCTCAG CTCAGCGTCA TCAAAGAATT GCAAAGTAGA GAAGAAAGCG 300
GCTGATTACC AAGGACGCCT TGGGCAGTGA GGAAGGGGGA GGGTGAAGGG GAGCCAATAT 360
ATGTGGGCTC CCAGGGTAGC CAGAAGGCGG CCCTCAGCAG TATCTAGGGA GCGGGAGAGA 420
GGGACAGGGG GTCGGGGGAG AGAGAGGAGG AGAGAAGAGA GAGGGGAGGA CGGAGAGAGA 480
GAAACCTGTG AGGATTCAGA CCGATGCCTG GGTGAGACTT TGAGGGCTGG GGACCGTGAA 540
TATGGCTCGC TAGCCTTCCT GTGGTCCCTT 570
|
