Tag | Content |
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EnhancerAtlas ID | HS002-01033 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:205409500-205410880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:205410208-205410229 | GAGGGAGAGGGGGCAGGAGAA | + | 6.39 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_57284 | chr1:205409616-205410328 | VACO_400 | SE_57284 | chr1:205410505-205411560 | VACO_400 | SE_57992 | chr1:205409731-205410388 | VACO_9m | SE_57992 | chr1:205410425-205410802 | VACO_9m | SE_68807 | chr1:205409040-205411834 | H9 |
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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 |
GH01I205440 | chr1 | 205409221 | 205412555 |
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Enhancer Sequence | CACCTGGCCC AGGAGGATGC TGGCAGGGGG CTGGAAAAGG ATTCTTGCCC CAGGTCCTGG 60 AATCCCAGGA GAGTCTCACA CTTCCGCCCT GGAGGCCTTC TCCAGGGTCA GGGCTGCTGG 120 AAGTTCTCTG CTAGAGCAGC CAGTTTCCCA TTTAGCAACA GCTCTCCTAG CCCAAGGCGG 180 CACATGCCTC ATGCGGTTAC CCTGAGAAGA GTCCCCCGAA GCTCTCAGGG CAGGAAAGAA 240 GTTTCACTCC TTGGCCTCCC TGGGGCTTCT CAGTCTCTGG AAGGCATGCG GCAGGTCCTG 300 GGGTTCCCCC TTGTGTGGCT GGGGCCTCTC TCCAAGGAGG TCTGAGAATT GGAAGCTAAT 360 GGGTGTGGGC ATGAGGAGGA TGAGAGGCAC ACAGGAGGCT GATGCCCTCG GGTGAGAGTC 420 AGGCTGAGAA GAGCACTGGC TAAATCAAGA CTTAAGATAC ACACACGGCT TCCTGCTCCA 480 AGCCCCAGCC AGAAGCAGGC ACCATCAGGC CTGGGACCTG CTGGGGGCTT GATGGAGGGG 540 CCCTGGTTCT GATCACACCG CCGTCTCCCG CTCTCTGTGA ACTTCCTCCT TCTTCCTCTT 600 CATTTTGCAG AAGCCGTGGA GACCACAGAA GCAGGCGAAA GTGAACTGGG GCATGCCCTA 660 CGCCAGGCTG GGGGAACACT CACCAGAGAT CTGCAGGGAA AGGCAGGGGA GGGAGAGGGG 720 GCAGGAGAAA GGCAGGAAGA GAGAAGCAAG CTGGGGTTAA TGCTCCCAGA ACCCTCTGGG 780 TCTGGCCCAG TCATTGCCAC TCCCTGAGGC GGCCCGCTAG GTCTCTCACA CCGGCTGGGG 840 GAGGAGTCAA GCCTCTAAAC AACAGCTCTT TGAAACCTCA GTGTTTCCTG ATCTGTGTGG 900 AGCTGATGTC ATTCCTCACA TTGGAGACAG GGTGAGTCCA AGGGAGGAAA GAGAATGCCC 960 AGCTGCTGCC TCCTTTTTTC CCCTCCCACC CGCTCTGCCC CACCTCATCA CCATATACCT 1020 GTGGTTGGGG AACAGGAAGC AAGCTGGCTT AAAATAGCCT CCGGCTTGTG CCACCTTACA 1080 CCAGGTTCTA GCTGGGGGCT TCCACTCGCT TCTGCAGGTT GCACACACGA CAGGCCCTCC 1140 TCCATCCAAA TGCGGACCCC TTCATCCAGT GTAGCTTTAC TTTGACACCT GGGACCGAGT 1200 CAGATTCCTC CCTTCCTTAA CAACCCCAAG TTGTCTGACA CCCTAGGAAA GCCTATAGGG 1260 AGCAATTATA CCCTTCCTTT GACTGCTCAG GGCAATGCAA ATCCCATCCT CACCATGCAG 1320 AGAAGAGACA GCAAAGAGGG TTCTTTTAGC CAACAGGCTC TTTTATTTAG CACCTATGCT 1380
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