Tag | Content |
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EnhancerAtlas ID | HS184-16003 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:20407730-20408670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr2:20408102-20408113 | TCTTGTTTACA | + | 6.02 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_02914 | chr2:20407353-20409539 | Bladder | SE_23108 | chr2:20407449-20409559 | Colon_Crypt_1 | SE_23761 | chr2:20407582-20408957 | Colon_Crypt_2 | SE_24805 | chr2:20407649-20408942 | Colon_Crypt_3 | SE_26530 | chr2:20403978-20426236 | Esophagus | SE_28384 | chr2:20407358-20409558 | Fetal_Intestine | SE_29057 | chr2:20406148-20409772 | Fetal_Intestine_Large | SE_31478 | chr2:20407303-20419416 | Gastric | SE_33954 | chr2:20407406-20409301 | HCC1954 | SE_35878 | chr2:20404964-20426386 | HMEC | SE_41823 | chr2:20404831-20409818 | LNCaP | SE_42432 | chr2:20403633-20409872 | Lung | SE_43614 | chr2:20404132-20426415 | MM1S | SE_50296 | chr2:20404815-20409905 | Sigmoid_Colon | SE_52465 | chr2:20407277-20409713 | Small_Intestine | SE_64257 | chr2:20407485-20409929 | NHEK | SE_67169 | chr2:20404132-20426415 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TCTCCTGCTG CACCGCCTCC CCCAAGAGAA AGCTCAAGAT GGGGCAGGGA TGGGGCAAGG 60 CACTGGCACT TCGACCCCAC GAGCCTCTGC TGCATTGTAG AGTGCCGAAT CTTTCAGCAG 120 AAGCTAGAAC CATTGGATCC ATGCTCCATT CAACAATGAG GCAACCGAAG CCCACAGGGA 180 AGACACACAC ACTGGGGCCC ATGTACAACC TGGGAGACAC CGCCCAGTGA GACCCAGGAA 240 CGCCAGGGAG GCCCCAACAC GTTAGCAGTT TCCCAAGAGC AGGGCTTTCC TCCTGACTAG 300 ATAAGCATTT CAGTCTGCCC TGTCCCTAAA AACAATTTGT TCCCTCAGTT CGGCTGGCTT 360 ATCCCTCTGC AATCTTGTTT ACACAACAAG CTCTTAAGCA AATGTTTTCT CCACTGAAAC 420 CAGCTCCCTG GCCTCCGGGG GCCTCTCCCC TCCCTGGGCC TTCAGTCTCC ACTAAGGGGA 480 CAGGCTAGAG AGACCTCCCA AATCTTCTCC AGCTTGAATC TTCTGGGACA GCCCCTCAGA 540 TGAGAAGGTG AGATTTCAGC CCCCTGAGGA GGAAATTAGC AGAAACTGCT GAGTTTGAAC 600 TTGGATTACC AAGGTGCCAG CTGACTCCCG GAGTTTCTGG TGAGACTTTC GATTTCCTTT 660 AGCAGGCCTG CTGTGCTGAC AGCCGGCAGC AAACTCCCTC TAGGCCTCCT GGGTAGCTCT 720 CCCCAGCATC ATCTCCAACC TGGGTGCTTC CGAGGCTGCC TGGCCACGGC TCAAGGCTGC 780 TCAGGAACAG GTGGCCTCAG CTTGGAGACT ACCTAATGCC CTGCCCAGGA AGGCAACAGG 840 CTAACCAGCC TTTAACCTCT GTAAGTCCCA GGAAAACCAA CTGTTCATAG AACGAATCAA 900 CAACTTTGTG CTAGGTAAGA TCTAGGCTTC CACTCATTCT 940
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