Tag | Content |
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EnhancerAtlas ID | HS095-14189 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr18:77218090-77219330 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:77218692-77218710 | GCTGCCTTCCTTCCTGCC | - | 7.34 | ZEB1 | MA0103.3 | chr18:77219147-77219158 | CCCACCTGCGC | + | 6.62 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_11551 | chr18:77215863-77229495 | CD20 | SE_58360 | chr18:77195352-77289402 | Ly1 | SE_61778 | chr18:77193611-77227418 | Toledo |
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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 |
GH18I079457 | chr18 | 77217644 | 77222092 |
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Enhancer Sequence | TCGGTGTGAA AGGGCTGTGG GTCACAGGGT GGCTCCGTGT GAGGCCCTGC AGGCAGATGT 60 GCAGCAGGGC TGGGTGGCTG TTTCCCCTCC AGAATCTCCT CTGGGAGCCA GGCTGGGACA 120 GACTCCTGGG GGAGAGCCGG GGATGGATGA GACGCCCCAG GGACGCTCGC TTCTGGGCAT 180 GAGGATGCTG TGGGGTGCAC GGCACGAGGA CGCCGCGGGG AGCAGGGCAC GAGGATGCTT 240 TGGGGAGCAG GGCAGGAGAC GCCGTGGGGA GCAGGGCTCG AGGGCACCGT GGGACCCAGG 300 GACGCTGCTG CTTCCACCAG CGGCCCTCGT GGCTTTCTTT GTGGAAACAG TGGCTCAGCA 360 TCAGCACCGG CGTGGGGGTG GCCCGGCTCC GGGCGGCGGG TCCTGGCCGG TCTGGGAGGC 420 TCCTGGGCCC GCAGGCCTGC CTGTGTGGAA ACCTCGCGGG TGTGGCAGGG AAGCCTCCCG 480 ATGACTCAGA CTGCAGGGAA TTCCCTAATG ATCTGGAATA TTTTTACTCC TGCACTCGGG 540 CAGTTTCCTA CTAAGGACTC GGAGCTCTGA TAAGGCTGAA CACAAAGGCC CTTTCAGGAC 600 CGGCTGCCTT CCTTCCTGCC AGGGGCTGAG TTTTGAACAG CACGGGGGCC GGCGCTGCCC 660 GTCCGGGCCT CCACGGAGCT GGGAGCCGCC ATGGCGATGC TCTTGCCGGC GGGACGCGGC 720 CCTGCGTCTC CTTTCCTGAG ATGCGAGGTT ATTTCCATCT TTCAGCAGTC TCGGCGCTTT 780 GTCTTGTTCT GGAAGCAATT GCTAGATAGA CATTTCTGGC CGTGAATACT ATTGCTTTTG 840 AAAGACAATT ACTTTATGAT CCTTAAGCAG AAACAGAAAG CCTGCCCTCA CCCTCACCCT 900 GGTCGACCTG AAACGGCCAC AGACGTCGGA CACCACGGGG AGAGGCCCCA CCTCCAAGAG 960 GGAAGGCCAC AGGCGCTGGC TCAGCCGGGG TCTTTGAGGA AGGCAGGGAT GTTTGTCGGT 1020 TCCCCGCACT TTTAGGGGAA GTCTAAGCGT ATCTGCTCCC ACCTGCGCAG GAATTGCAGG 1080 GTGCGGGTGC TCCCAGGTGT GCGGTGGAGG CTGCTCCATG GCAGCTGCTG AGCTGGGCCT 1140 GGCTGGCCAC GCAGACGTGG CTCCCCTTGG GGCCGCTCCG GCAAGGATGG TTCCCCACAG 1200 GCCCACGAGG CACGGGTGGG AAAAGACGCC TCCATGCCGT 1240
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