Tag | Content |
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EnhancerAtlas ID | HS184-19213 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:24255660-24256580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:24255933-24255951 | ATTTCCTTCCCTCCCTCC | - | 6.45 | KLF16 | MA0741.1 | chr22:24256256-24256267 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr22:24256352-24256363 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr22:24256257-24256267 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr22:24256353-24256363 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr22:24256351-24256366 | CGGGGGCGGGGCTTG | - | 6.23 | ZNF263 | MA0528.1 | chr22:24255838-24255859 | CTCTTCCCTTCTTCTTCCTTC | - | 6.61 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_37758 | chr22:24249966-24257197 | HSMMtube | SE_56738 | chr22:24255405-24256233 | VACO_400 |
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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 |
GH22I023907 | chr22 | 24250157 | 24258315 |
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Enhancer Sequence | CCTGACTCAG ACCAAGACAG CTTTTGTTTC TTTTCCTTTC TAGCCCCCCA CTTCCCACCC 60 ACCTTTCTGC TTTCTCATAT GGGCTCATTA TGGTTTATAG GGCTGGGGAA CGTTGCCTCT 120 TCTGCCCTCC ATTTCTCCCA TCTCCCTTCT TTCCCCTCCA CTTTTTCTGA GTCCACTTCT 180 CTTCCCTTCT TCTTCCTTCC CTCTGGGACG CTGCACAGTT CCTTCCACCC GGCACGGCCT 240 GGGACTCTAG ACTCCCTCTG AAGGCACGGA AGTATTTCCT TCCCTCCCTC CGACCCGATC 300 TTTCTGCCCT TGATTCAAAA CAATCTGAGG TCCCTAGGCC CTTCCCTTTC CGCCTCTGCG 360 CTCCCCATGG GGTCCGGTGT AGTTTTCCCG CCCCTTCCCT GCAGCTCCCG AGACCACCCG 420 GACACAACGG AGCCATCCAG CGCCCTCAGA GGCCCTGGGC ACACGGGCAG ATGGTCACCG 480 CCTCCTAAGG GAGCAGCGCG CGCCCGTTGC TCGCTGCCCG TTGGTTGTTG CTGGTAGCTC 540 CGGAGGGCGG GGTTGGCGAG GAAAGTGAGT CCGTATGTCC CCAGCATGCT CCGCGCGGGG 600 GCGGGGCTCT AAGGGGGCAG GCGAAGGCGG AACTGGCGTG GTCAAACCAA CCTATCAGCC 660 TCCAGCATGC TCCGTGTGGG AGCGGGGTTC CCGGGGGCGG GGCTTGGTTT GTGTGCCCTT 720 CCGGCGTTTC GCCCCTGCGT TCTCTGAGAT GCTCCCACGC AGATGTATGG GCCTAATTCG 780 CTAATATCCA CTCTATATCC TGTTCCATCC TCTTGTAATG GGCGTTTGGA GTGTTGCCAA 840 TTTTTTGCTG TTATAATGAT TGTAATAGCA TATTAAAAAA CTTGAACATA GTTTGATTGT 900 AATAACATTA AATATAGCAT 920
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