| Tag | Content |
|---|
EnhancerAtlas ID | HS158-09598 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr11:12387540-12388440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr11:12387964-12387980 | CACAGTGTAAACAAAG | + | 6 |
|
| | 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 |
| GH11I012366 | chr11 | 12387548 | 12388368 |
|
Enhancer Sequence | CCGGTTTGCA GCTCCTAGCG AGATCGATAC AGAAGACAGG TGATTCTTGC ATTTCAAACT 60
GAGGTATCTG GTTCCTCTCA TTGGGACTGG TTGGACAGTG GATGCAGCCC ATGGAGGGCG 120
AGCTGAAGCA GGGCAGGGCA TCGCCTCACC CAGGAAGTGC AAGGGGTCAG GGGACTTCCC 180
TTTCCTAGCC AAGGGAAGCC ATGGCAGACT GTACCTGGAG AAACTGTACA CTCCTGACCA 240
AATACTGCGC TTTCTCCACA GTCTTAGCAA CTGGCAGACC AGGAGATACC CTCCCATGCC 300
TGGCTTAGTG GGTCCCACGC CCACGGAGCC TTGCTCACTG CTAGCACAGC AGTCTGAGAT 360
CGACCTGCGA TGCTGCAGAT TGGCGGGGGG AGGGGCGACT GCCACTGCTG AGGCTTGAGT 420
AGCTCACAGT GTAAACAAAG AGGCCAGGAA GCACGAATTG GGTGGAGCCC ACTGCGGCTC 480
AGCAAGGCCT ACTGCCTCTG TAGATTCCAC CTCTGGGGCA GGGCATAATA GAACAAAAGG 540
CAGCAGACAG CTTCTGCAGA CTTAAACATC CCAGTCTGAC AGTTCTGAAG AGGGCAGTGG 600
TTCTCTCAGC ATGGTGTTCG AGTTTCGAGA ACGGACAGAC TGCCTCCTCA AGTGGGTTCC 660
TGACCCCCGT GTAGCCTGAC TGGGAAACAT CTCCCAGTAG GGGCCAACAG ACACCTCAAT 720
CAGGCGGGTG CCCCTCTGGG ATGAAGCTTC CAGAGGAAGG ATCAGGTAGC AATACTTGCT 780
GTTCTGCAGC TTCCGCTGGT GATACCCAGG CGAACAGCAT CTGGAGTGGA CCTCCAGCAA 840
ACTCCAACAG ACCTGCAGCT GAGGGGTCTG ACTGTTAGAA AACTAACAAA CAGAAAGGAA 900
|
