Tag | Content |
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EnhancerAtlas ID | HS095-10865 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:2280280-2281470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr16:2280487-2280497 | GGGGCGGGGC | - | 6.02 | REST | MA0138.2 | chr16:2280454-2280475 | GGAGCTGTCTAGGGACCTGAT | - | 6.01 |
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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 |
GH16I002230 | chr16 | 2280528 | 2282095 |
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Enhancer Sequence | TGCTGTGGGA GGGGCTGTTG CGAGGTCTGG ATGGGCAGGC TCTCATCGGG GACAGATGCT 60 TGTGCAGGGG GGCATTCAGA GGCAGCCAGG GCCTGGGCAG GTTGAGGGAG CTAGGGGCTG 120 CTGGGGTTGG GGGTGCGGCA GGGGCGAGTG GCTAGGTGTG CAGACGCGAG GGAAGGAGCT 180 GTCTAGGGAC CTGATGCTGT GGGAGGTGGG GCGGGGCATG GCTGCTGCCT GGGGAGCCTG 240 CTGGACCGGG GCTGAGGCAG GCGGGGAGTG GGCAGCTGGA CAGGAAGTAG GTTTGGGCAC 300 CAGGCGGAAC CTGGCCTTGG GCAGCCCTGG GGACTGGCTG CAGCAGGAAG AGGGGGTGGA 360 GGAGCCGTGG CGGAGGCCAA CCCGGGGCCT GGGAAGGGCA CCTGTGAGCA GGCTGCTCTC 420 CAGGAGGCAG CCAGGGCACC TGTCTCACCT CCGTGCTGCC TTTCCCTGGC ATTCCTGCGA 480 CCAAGACACT CATCAATGCC ACTCAGAGCT CGGAATGTTC ATGTGGGAGG TGGGGCGGGC 540 TCTGGCCTTG ACCTGGCGTT TGGTTTCTGG GATGGTGGCG TCACCTGGGA GCATGAACTC 600 CTTAGGTTCT GGCGGGGTCT CTGGGCTGGG TCTCTGGCCA GCCAGGCCCC TTTCCACCCA 660 CCTAAACTCT AGCAGCCTCC AGCCCTAGGC TCAGCACCCC TCCCTGTGCT TCAGCAGCCC 720 CTCTTGGCAC CCCTGCCACT CTGGCACCCC TGGGATTTTC CCCTTTGCGG GCATCCTGGG 780 TACTCTGTGT GTGCCCTTGG CCAGTCAGCA GGCCCGGTGG GCTTAGTCCA GGGCTGCTAG 840 CTCTCCTGTT GGCCTCTAGT GGAGATGGCA GAGGGTCCTG CCTGCTGGTG GCCAAGGGCT 900 GGGGCGTGCC AGGTCCTGTC TTTGCGGGTG CAGGGGTGCG GTCAGCTGTG TGGGCAGTTG 960 GAACCCACCT CCAGGCCCTC CTGCCGCTTC GCGGAAAAAG TTCGCGTCTC CTCTGGCCTC 1020 GCAGCAGCCA TGTTCCCCCA GGTCCTCCCC ATCAGAGGCC TCTGTCCTTT GGAAGATCAC 1080 TCCTGGGGCA TCGAGCGTGT AAGGGCTCGG GCAGGAGAGG CTCTTAATTG TTTCTGAGTC 1140 ACCACGCTTT TGTCGTGTTT CAAGAGAACA GCTTGTCAAA ACAAGACGCC 1190
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