Tag | Content |
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EnhancerAtlas ID | HS133-20708 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:45222270-45223390 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr21:45222628-45222649 | CTTCCTTCCCCTTCTTCCCTC | - | 6.31 |
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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 | AGGACTAGGG GGTGTGTTAG TCATGGAGCC GGCGTCCTCA CCTGCTTGCT TCTCCCCTGG 60 ATGGGGGTCA CCTGCAGTGT CTCCCCCTGA AGCATGAGTG CCGAGTCCCC CATCCTGGGT 120 GCCTGCTATC CACGCATCCC GGAAATGCCC TGTCCTCGGC ATCCCTCCTG TAGGCCTCTC 180 CCTGCCTCCC CCACCCACCT TCCTTGTCTG CAGCTCCCCC GAGCTGTGTG CGCTGCCCTC 240 CCTCCCGGTC TGGAGACATC CTCCTGGCTG GGCTGCCTCC TTCCGTGCCT CCGTCTTAGA 300 TCCAAGCCCC GTCCGCTCCT CTCCCGCACC CTCCAGAGAT TCCTGAGTCT CTCCACGTCT 360 TCCTTCCCCT TCTTCCCTCC ACTTCTTCCC TCCACTTCTG TCCTTGATTT CTGGGGCTGC 420 CTTCCGTGTT GGGCCTCTGG CCACACGAGT GTGGTTGGCA TGTGATGCCC TCACCAGGGG 480 CAACCCTGGG TCCGCGGCAG ACCACTCAGG GCCTGGAGCT GCCTACCTGC AGTGGAGGGG 540 GTTGAGCACA GTGCCGGGCA GGGCAGGGGG CCCATGGCAA GAATGGGGTG CAGAGGAGGC 600 ACATGGTGGC TTTGCCCCAC ACTGGGAAGC CTTCCCTGTT ACTCTCTCCA TGCTAAACTG 660 GCCCCAGGGC CTAGGGATTC ACCCCTTCCC TTGCCCAGAG CTCCGTGCCA TTGAAGCCGT 720 CCATCTCATT TCCCATGAGG CAGTGGCCTC CTCTTTGTAG CCGGCCCTTG GCTGTGTGAA 780 CCCTGTCGGC CCTGGCGTTC AGGACCTGGC ACTGCCTGGC GTCCTGTTCT TCCACCTCCC 840 CTTCTGCCTT GAGCCCAGTC CTGCCTACTC CTCTGTGCCT TTGCTCCTGG GTCTCATGAC 900 CCTGTCCTCA CGCTGGTCCT TCTGAGGTCA GCCCTTGCTG AGGTCCTGAG CCGTGTGGAT 960 GGAGCTTGGC GCCCACACTG GACACGGGAT GCGTCTGGCT GGCTGTTGTG GCCGTGTTGT 1020 CCTCCCAGGT CTGTGGTGCT GGCATCCTCA GCCTGAGTTG GAGTAAGTGG AAAGAGCCCG 1080 TGTTGGCATT CTCTGGCTCA TGGGGTCTTG CTGTTTTGTC 1120
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