Tag | Content |
---|
EnhancerAtlas ID | HS158-11586 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr11:111198520-111199580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr11:111199192-111199203 | GGATGACTCAT | + | 6.62 | JUNB | MA0490.1 | chr11:111199192-111199203 | GGATGACTCAT | + | 6.62 | NFAT5 | MA0606.1 | chr11:111199441-111199451 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr11:111199441-111199451 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr11:111199441-111199451 | ATTTTCCATT | + | 6.02 | TEAD1 | MA0090.2 | chr11:111198806-111198816 | ATGGAATGTG | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_31835 | chr11:111197996-111199688 | Gastric |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 111198606 | 111199234 | chr11 | 111198652 | 111199238 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH11I111327 | chr11 | 111198701 | 111198850 | GH11I111328 | chr11 | 111198886 | 111199232 |
|
Enhancer Sequence | GGAGGCCTGG AGAGATGAGG TGGCCCACCC AGGGTCATAC AACTAAGAAA GGTAGAACAG 60 GATTCAAATC TAGGTCCTCT TACACCAGAC CCAGTGCCTG TCCCAGGGTG CCGTCAGTCC 120 CATTGCTGCT GGAGGGCAGC ATGAGTAGCA CACCATCCTG CCAGCCGCCC TCTAGCCAGG 180 GCAGACTCTC AAAATGCAAA ACTTGCCAGA CAGGCAGGAA TGCAAATGCA CACACAGCCT 240 GAAGTAGATC TGCCCTGACA GAAGTCACCC AGGTGGCCAC TTGGCCATGG AATGTGCCCA 300 GCTTGATAAG AAGGCAAATG CCTGGCGTCT TGCAGGGCCA GGGTGCATAT CAGGTTTCAT 360 TTCTGGGCTG TGGCAAGACA GAAGCCGTAT GTGGTCTTTG CCTGCCAGGA CTGGCTGGCC 420 CTGATGCCCA CGGCCTGCCA GGCATGACAA GCCCAGCAGT CTTCCCTAAC GGGGCCTTCT 480 CTTGCCCCAA GCAACAGTCC TAATGTCTTC CAAGTTGGGC ACAGTTCCAC AGCCCCATAA 540 AGCTGCAAGC CAAGGAATGC AGCTCCCTTT TACTTCTGCC TTTCTGAACT CTACCCTTCT 600 TTCAAGGTCA GCTCAAGCCT GCCCCCCACA TTACAGGTTA GGTTCAAATG CCAATTCTAG 660 CTGTATGGCC TTGGATGACT CATTTAACAT CTCTTAGCGC CCTTTTGTGA ATAAAATGGG 720 CGTAAAAATG TCCACTCCCC AGGGCTATGG TAAGGATTGA GAGGCCCAGT GAAACTTCGC 780 ACATAGTATA TGCACAGTAA ATGGTAGGCA GCCCCCACTT CTCATAGTGA CCTCTCTTCC 840 CTGCATTTCA GTTTCTCTTA TCACCCGCCT AATTCAACTT AGCATTTTAT TAAACACTGA 900 CTCACATCTG TTTAGCTCAT CATTTTCCAT TCATGTGTAA GTCTCGTCTT TCTCTGATCT 960 TCTTAGAACC AAGAACCAGG CTGTTCTTTC TCTCATTTCG CCATGGACCA CTAAGCACAG 1020 TTTGGAATCG TCACATGACT TATCAGTTGC TGCTGGTGGG 1060
|