Tag | Content |
---|
EnhancerAtlas ID | HS158-09562 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr11:11879100-11879760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:11879670-11879691 | GTGTACTTTCGTTTTCAGTAC | + | 6.24 | NFYA | MA0060.3 | chr11:11879328-11879339 | AACCAATCAGA | + | 6.62 | NFYA | MA0060.3 | chr11:11879483-11879494 | AACCAATCAGA | + | 6.62 | NFYA | MA0060.3 | chr11:11879463-11879474 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr11:11879323-11879338 | AAAGCAACCAATCAG | + | 6.7 | NFYB | MA0502.1 | chr11:11879464-11879479 | CTGATTGGTTGCTTT | - | 6.7 | Pou2f3 | MA0627.1 | chr11:11879420-11879436 | CTTCATTTGCATAGAA | - | 6.48 |
|
| 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 |
GH11I011857 | chr11 | 11878975 | 11880618 |
|
Enhancer Sequence | GATTTTAACA CTGGAAGGGA GGCAGTAGTT ATGAGGCAGG AGAATAGAGT CTGGACTCAG 60 GAGCTTAAGG CCATTTCACG CTTACTTCTT AGAACTAAAT TGAAAGGAAA ACCCTCACTT 120 TCCATGCCTA AGTAACAAAA GAGCCGGAGG CTACTCCCTT TGCAGACCCC TACCTTTTCT 180 GCGTGGCAGA TGGAAAATTG AAAGTACCTC TGGTTGGTTG CAGAAAGCAA CCAATCAGAC 240 GTTTGCAAAG GAGTGTAACT TTGTAACTTC GCTTCAGCCT CTGGTTGGTT GTTGGCAAAC 300 AGACTGATTA CGGGCCAAAT CTTCATTTGC ATAGAAGTGC AGCTTTGTAA CTTCACTTCA 360 GCCTCTGATT GGTTGCTTTC CACAACCAAT CAGATGTTTG CATAGGAGAG TGACCTTTGT 420 AGCTTCACTT CAGCCTCTGA TTTGGCACCA CTTCATTTAC ATGAGGTGAA TACCAAGTGA 480 CCAATGGGAA ACCTTTGGCA GGTATTTGGA CCCAAGAAGA TTCTGTATCC AGGCCCTTTA 540 GCCGCTGCTG GTGCAGTTCC CATTAGTGGA GTGTACTTTC GTTTTCAGTA CATCTCTGCT 600 CTTGTTGTTT CATTCTTTTC CTTGCTTCTT TTGTACATTT TGTCCAATTC TTTGTTCAAA 660
|