Tag | Content |
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EnhancerAtlas ID | HS184-15365 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:18851970-18853050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:18852821-18852839 | CCCTCCTTCCTGCCTGCC | - | 6.66 | FOXA1 | MA0148.4 | chr19:18852048-18852064 | CATAGTGTAAACAAAG | + | 6.08 | MSC | MA0665.1 | chr19:18852601-18852611 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr19:18852601-18852611 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr19:18852601-18852611 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr19:18852601-18852611 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28464 | chr19:18847206-18855188 | Fetal_Intestine | SE_65614 | chr19:18849682-18858357 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 18852466 | 18852975 | chr19 | 18852715 | 18852875 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I018736 | chr19 | 18847339 | 18855023 |
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Enhancer Sequence | CTTGGGAACC ATGAGAGTTC TGTGTGTCCC CAGTCCTGTA GATTGTCCCC GCATCCCAGG 60 TTTCCTGTGG CCCGGGGACA TAGTGTAAAC AAAGCTGCTT CAGGGAGTTC TTGCCCCTGA 120 TGTCTGGCCT CCTGGGAGCT GGCAGCTCAG CCCGTGTAGA AAGCACATGT GGCATGAGTA 180 CCTGCTGTGT CACACGTCGT GTGTCCCTCT CACACCCGCC TGTAGCACTC ACTCTAGGTC 240 GGGGACACAG GTCCAGGAGG GGTCACAGCC TTTAGGGCCA TATAGTCAGT GAGAGGTGAA 300 TGTAGCACAG GTTTCTGTCA TGCTACTTGG ACACAGAAGA GGGTGGAGAA AGTCACGGGA 360 GGCCACAGGC GACCTATGCC CAGGTAGGTG TGGGGTGGGA GCTGTAGGAC CCCCACCCTA 420 CACCCCCTCC CTCTGCCACA GCCCGGAGCT GGCCTGTTTC ATCTGGTGTG ACTGCTGGGA 480 GGGACACTGT GGATGTTCAT TGTGTATGTG TCTGGCCAGC GGCCACCAAG GGCTCCCAGC 540 ACAGACCCTG GGCCTCACCC CCAGGCCCTC GAGAGCCACC CAATAACACA CAAGGTTAAT 600 CTTACCATCG GCTCCACTTC AGCTCACAGG AAACAGCTGT TTACCTGGGC GAGGTGCTCA 660 GCCGGGCAGG TGGCCAGTTC CCGGGCTTTA CTTCCGCCTC CGGTGTCCAG GGCCCCCTAG 720 GAAGCTGGGG CGGTGGGGCA GCCAGCTCTC CACGCACTGC CAGGAGCTGT TTGTAAGGAA 780 CGAGTCGGCC TTGTTGTGTA CACAGTGTCC ACCCTAGCAA CCGCCCCTGC CGGGCCAGAG 840 TGGACAACCA CCCCTCCTTC CTGCCTGCCC AGCCCCACCT CTCCTCACGG TGGCTGCCTC 900 CCCCAGTTGC ATGGCAGGCA TCATGGACCA GCATCCCCAA GGGCCTCGGG TCGTGCCACA 960 TGGGTCAGGG GCCTCTGTTA CTGGCAAATC AGCATCAGCC ACATGAAGGG GAGGAGGCCA 1020 GCTTCCAGCC CTGTTCAGAG TCAGCGTGAC CCATCAGGGA GCTCCTGGCC CCTGGTTCTG 1080
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