Tag | Content |
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EnhancerAtlas ID | HS133-20805 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:47330130-47330810 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr21:47330589-47330599 | GGTGCCAAGT | + | 6.02 | SRF | MA0083.3 | chr21:47330135-47330151 | TGCCCAAATATGGGCC | - | 6.04 | SRF | MA0083.3 | chr21:47330135-47330151 | TGCCCAAATATGGGCC | + | 6.26 | Spz1 | MA0111.1 | chr21:47330773-47330784 | GCTGCTACCCT | - | 6.02 |
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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 | CCCACTGCCC AAATATGGGC CCTTTCCACC CACTGCTCAC CTATGGATCC TGCCCACCCA 60 CTACACTCCT ATGGGCCGTG CTGGGGACAG GGAGGAACTA GCTGGTCACA TGGTTCTGGG 120 CAAGGGAGGC CCTGGGCACT GGGTGCTGTA TCTACTCCCT GTGAGGGGCC TCCAGGGCAC 180 CTGGAGACAG CCCTGAGCCA TCGGCCTGTC CCAGTGGGCA GAGTTTGCAG ATGTGAACTT 240 CACATCCACA CGTTTGTCCC ATTTCAAGGA AAGCCTGAAT CCTTGCCCTA TGCAGCAGGG 300 CAGCTGCCCC AATCTTCATT TCCTTTCCCA TGACCAGAGT CCACCTTTCT CTGTGACCTA 360 AAACTCCACA GAGGAGAGAG GATTCCGTGT ATTTGAAAAG AGTCGTTTGT CTCCCTGAAA 420 ATGCCTCTGA TTAGATGCCT CCTTGTCTAG CCTTGGCCAG GTGCCAAGTG CGCCCGAGGG 480 AAGGCACAGG GCCGGGTGCC AGGCCGTGGT AGCAGGGGCA GCATGGGGGC AGTGCTGGGA 540 TGGCGGTGGG GGAGGGGGCG CGTGGGCTGT ATGCAGGTTT CCAAGGAAGT GTCCCCCGAG 600 CTGCCTTGGG TGCCGAGACT CGGGAGGTAC TGCTGCCCCA TGCGCTGCTA CCCTGGTGCT 660 CCCTTCCAAT GTCCCCTCTC 680
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