Tag | Content |
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EnhancerAtlas ID | HS012-21900 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr7:130008620-130009620 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr7:130009276-130009287 | CTTCTGGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr7:130009276-130009290 | CTTCTGGGAAATGA | + | 6.44 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00149 | chr7:130002553-130015015 | Adipose_Nuclei | SE_29825 | chr7:130004187-130015191 | Fetal_Muscle | SE_34035 | chr7:130008358-130014926 | HCC1954 | SE_38986 | chr7:130008090-130010388 | IMR90 | SE_45274 | chr7:130008308-130010271 | NHLF | SE_54060 | chr7:130008287-130015096 | Spleen | SE_65534 | chr7:130002719-130009567 | Pancreatic_islets |
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| 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 |
GH07I130362 | chr7 | 130002564 | 130015278 |
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Enhancer Sequence | AGGGGACGAG AGGCTGCTTC TCATTCCGCA GGGGAGCCTG AAATGTGGGG GAAGCCTCTG 60 CACTCTCCAG TCTACCTTCA GGAAAATAAG GGGGTAGAGG CTGTAGCTTT TCTCCTCTTG 120 CAGTGTTTTC AGGGCCCGGA ACACAGAAGG CACACATTGT CCCAGCATAT TTACATTTTA 180 AGATGCTCCT GGAGGGGACA ATGTTTGCTC TAAAAGAGCA TTTCTGATGG GGGCATTTCT 240 GCCACCTTGA GGGAAAGGTT GGCCCAGACA GGCCACCTCT GCCTCGGTTG GCTTCACTTC 300 CCATGCAGGG AGGGAGCAGG AGCACATTTT GGAGGTTACC ACTCACCCCA CAACCCAACA 360 CGAATGAGTC ATTGGCTTAT GACCTGCTCC CCCCGAGGTG TCCTCAAAGG CTCCCTGGGT 420 CTTGGGAACA CAGGGTCAGA GCTAGTCAGA GCCAGCACAT CAAAGCACCG CATATCCAGG 480 AAGAAGAGCT TCTCATCATC ATCATCAGCG ACACCATCCT GGTTGTCATC CCTGAGCTGT 540 GTTAAGTAGG CACTTCCCCT AAGAGAGTTA AAGGGGCACT CGTGAGATAC TAAGAAGACT 600 CCTTCCCCCA GCCCCAGGCC TCCTTGTACC TTTTGCCTCT TCATTCTGTC TGCTGCCTTC 660 TGGGAAATGA TGGGACTGGC AGGCTGTACT ATGCAGCAGG GATAGCAGGG CTGTTTGCTC 720 TGCCCTCAGG AAGGCAGATA ACCCCTAGAA ACAGGAAGAG CCAAATGAGG TTGTGTAAGT 780 CTGAGGCAGA AACATTAGTC GTGAGAGCAA GACTTGCATT TGCAAGAGCC AGGCTGTGTG 840 TGTGTTTGTG TGTGTGCGTG TGTGTGTGTG CATGTGTGTG CACGTGTGTG CATGTGCGTG 900 TGTGTGTCCG TGTGTGTGTG TGTAAAACTG GATGGCCAAG AGCCAACCCC TGGAGGGCAC 960 GGAGACAGGG AAGAAAACAG AGTGAAACAA AAATATTTGT 1000
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