Tag | Content |
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EnhancerAtlas ID | HS120-03603 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr2:20407740-20408690 |
Target genes | |
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 | CACCGCCTCC CCCAAGAGAA AGCTCAAGAT GGGGCAGGGA TGGGGCAAGG CACTGGCACT 60 TCGACCCCAC GAGCCTCTGC TGCATTGTAG AGTGCCGAAT CTTTCAGCAG AAGCTAGAAC 120 CATTGGATCC ATGCTCCATT CAACAATGAG GCAACCGAAG CCCACAGGGA AGACACACAC 180 ACTGGGGCCC ATGTACAACC TGGGAGACAC CGCCCAGTGA GACCCAGGAA CGCCAGGGAG 240 GCCCCAACAC GTTAGCAGTT TCCCAAGAGC AGGGCTTTCC TCCTGACTAG ATAAGCATTT 300 CAGTCTGCCC TGTCCCTAAA AACAATTTGT TCCCTCAGTT CGGCTGGCTT ATCCCTCTGC 360 AATCTTGTTT ACACAACAAG CTCTTAAGCA AATGTTTTCT CCACTGAAAC CAGCTCCCTG 420 GCCTCCGGGG GCCTCTCCCC TCCCTGGGCC TTCAGTCTCC ACTAAGGGGA CAGGCTAGAG 480 AGACCTCCCA AATCTTCTCC AGCTTGAATC TTCTGGGACA GCCCCTCAGA TGAGAAGGTG 540 AGATTTCAGC CCCCTGAGGA GGAAATTAGC AGAAACTGCT GAGTTTGAAC TTGGATTACC 600 AAGGTGCCAG CTGACTCCCG GAGTTTCTGG TGAGACTTTC GATTTCCTTT AGCAGGCCTG 660 CTGTGCTGAC AGCCGGCAGC AAACTCCCTC TAGGCCTCCT GGGTAGCTCT CCCCAGCATC 720 ATCTCCAACC TGGGTGCTTC CGAGGCTGCC TGGCCACGGC TCAAGGCTGC TCAGGAACAG 780 GTGGCCTCAG CTTGGAGACT ACCTAATGCC CTGCCCAGGA AGGCAACAGG CTAACCAGCC 840 TTTAACCTCT GTAAGTCCCA GGAAAACCAA CTGTTCATAG AACGAATCAA CAACTTTGTG 900 CTAGGTAAGA TCTAGGCTTC CACTCATTCT GTTGTTCAAA GCAAGGGATG 950
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