Tag | Content |
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EnhancerAtlas ID | HS064-09168 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr20:1850940-1852370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr20:1852003-1852021 | CAGGAGGGGGCGTGACCT | - | 6.06 | KLF14 | MA0740.1 | chr20:1852006-1852020 | GAGGGGGCGTGACC | - | 6.45 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 1851849 | 1852180 | chr20 | 1851023 | 1851600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I001870 | chr20 | 1851048 | 1857547 |
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Enhancer Sequence | ATTACCTTTT TAAAGACCCA ATCTCCAAAT ACAGTCACAT GCTAAGGTGT TGGGGGTTGG 60 GGCTTCAACA TATGAATTTG GTGCGGGTGG GAGAAGACAT AATTCAACTT ATATGGCATC 120 TAAAACATTC TGCCTAGGGC TGTCAGGTGT AAGTAAGCTG TGCTTCTCTC TCCACTGCCA 180 CCAGAGCCTG GGGCTGCGGT CAGTGGCTTG GGCTGGGCCT TTAGAGCCTG AATAAATCGG 240 TCATCAGATA TGAGCTGCCC AGGGAGGGGA CATGACCTCA GGCAAGACTG CTCTCCTTAA 300 CTGGGCAATC TCCAACAGGG ACTTTGCTGC ACCACCAATA GCTGGGCAGT AAGTCCTTCT 360 TTCCTGAGGA GAGCTGGGCA CCCACCCTGC CCCTTTACTC GCTACATGAC CATGGGTAAG 420 CTCCTTGCTT TCTCTGAGCC TCAACTTCCA AAACTGGAAA AAAAATAAAA TGACTTGCAG 480 AGGGATGATG ATGAGATGGG GTCATTGCTG GTATTTTTAT TTAGGCAACA ATTTATTTTA 540 TTGAGCACCT AGTATGTGCC AGGCATTGTT CTAGGCTCTG GGGATATAGC AGTGAATAAC 600 ATGGACAAAA TCTCAGTTAA AGCTGACGTC ATTACAGGGA CTGCCAGGCA CTAAACAAAT 660 AAGCAAGTAA AATACATAGC ATGTCAGATG CTGATAAGTG CTGTGAAAAA GTAGCAATTA 720 AACCAAGAAA GGGGAAGCGA GAGTGTGAGA GGCAGGGGTG CGGAAAGGGG GATGTCACAA 780 TTTTAAATAA GATGGTCAGG GAAGGCCTGT CTATGAAAAG ATTTGGCAAG GTAAGGGGGC 840 CCTCTAGATA TCTCCGAGCA GAGCTTTGCA GGCAGAAGGG CCGTGAGCAT CCCTGACGTG 900 GTTCCTGAAT GCACGGCCTG AGCTCAGTGA GCAAAGGGGA CCTAGACTGG ACATGAGGTC 960 AGAGGAGTGG CCGGGGTCAG CCAGGGCAGG GCCTGGCAGG CCACTGTCAG AACTTCGGCT 1020 TTTCCTCCAC ATGCAACGTG GAGCCACAGG AGTCTTCTGA GTGCAGGAGG GGGCGTGACC 1080 TCACTTTGAT TTTACTAACA CAGGGTAACC CAGGTGACAA GCTGAGATTG CAGCCGGCTC 1140 CCCTGCTCCC ACCTTCCAGC CCCGCTGGGC CCCACCTAGT AAGCCCTGCC CAAGCCGCCA 1200 CCCCCTCTCC ACACACACAC ACACACGCGC TCCATCAGTC CCACGCCTGC TTGTCCGTCA 1260 AGTCTCAGTC TAGCCCTCAC CTCCTCCTTT GGGAAGCCAG CCCAGAGCCC CTGACCTGCC 1320 TCATCCCTCC CTCCCCAGAG AACCAGGAGG CAGTTAGGGG ACAGGCCTTG GCAATCAAGC 1380 GCCAGATTCA AATCCTCCCT ACTTAGAATC TCTGAACCTC AGTTTTCTTC 1430
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