Tag | Content |
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EnhancerAtlas ID | HS087-06518 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr14:89770150-89771260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr14:89770650-89770661 | GGGCGGGAAGG | + | 6.62 | HOXA13 | MA0650.2 | chr14:89771085-89771096 | CCCCATAAAAC | + | 6.02 | MEF2A | MA0052.3 | chr14:89770413-89770425 | GCTAAAAATAGC | + | 6.44 | MEF2B | MA0660.1 | chr14:89770413-89770425 | GCTAAAAATAGC | + | 6.92 | MEF2C | MA0497.1 | chr14:89770411-89770426 | CTGCTAAAAATAGCT | + | 6.57 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_10408 | chr14:89768030-89775675 | CD19_Primary | SE_10986 | chr14:89767517-89777419 | CD20 | SE_30616 | chr14:89768522-89772874 | Fetal_Muscle | SE_32618 | chr14:89769263-89776041 | GM12878 | SE_68967 | chr14:89770185-89771777 | H9 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH14I089301 | chr14 | 89768208 | 89776143 |
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Enhancer Sequence | TGAGGACAGT CCTATAATTC ACTATTATCA GTGTATCTAC TTTAACTTGG AGCCCAGGCA 60 ACCAAGCACT AAATTAACAC TGCCCTGTCT CTGCAAAGGT GATGGGGGAC AAGACGCCTT 120 GTAACTTTGA AGAAGAGATT TACACACCCC TGTGTCTCCC ATATAAATGG ACTCAAGAGC 180 TGCAGCAGTC CATAAATGAT CCTTTCTTTC CACTGTTGAT AGTTGAAGGC AGCCGTTTCC 240 AGCTTCTTGC CGGTGATCAC TCTGCTAAAA ATAGCTTTGA TGCTGTCACA TGCAAACTTG 300 AACAGAACCT GAAAGCAGTT CCCCTTTTAG TTCTGAGCTG GTTCAACTTT AAAAGAGAGG 360 CAGCTGTGAA CACACTCCAG CGTGTTTACA TGATGCTGAA GTAGTTCAGC TCGTAGTAAA 420 AATACCACTG AAAAGGGACA GGCTTGGGTT TGCAGCCTCT GCTGACGACA TTTCTTCCTG 480 CTGAGCTGGA GCCCGGGAAG GGGCGGGAAG GGGCGGTAAG GTTAGCAGGG AAAATCCAAA 540 ATGTCCAGTT TGAAGGGGAA AGTGGCTGTG AGCAGAACCG CGGTGAAGAC AGGAGAGAGA 600 TGTTTGTTGA GATGTGAGAT TTCTGACTAT GGTGGAGGTG GGGGCAGGAG AGGCGGCAAA 660 GATCATATAG AAAAGAGAAC TTAGACAACA GGGGGTGCTT TTTAAAAATT CTGTTAAAAA 720 TATCTAAGGG CTGTTTTTTT AGAAATCAAG GAAACAAAGG ATGAAATACA TTCAACATCT 780 TGGCCATTCA TTTGATACCT TATGTTGGTT TGCTGGGCAA ATGGATGATT CTGGATGTGT 840 TCTGAAAACT GGGCCCAAAA CTAAGGATAA AGCAGAGTAT GGGCTTGGAA ACCAGAGAAA 900 ACCTGGGCAT TCAACCCGGC TGCTCCTCGT CTGGCCCCCA TAAAACTTGG CTTAAGCACT 960 GGTGTCTCCC AGACCTTCTG CACAGAGCTG GGAGTTAAGT GAGAAAATAC ACACCGAAGT 1020 GCCTGGTGGA GCGGGGGACC CTGACCCATA ATAGACAACG TCCTTTAAAA ACATATACCC 1080 AGAGGAGAGG AAGCTGACAG TGATCTGCGG 1110
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