Tag | Content |
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EnhancerAtlas ID | HS017-12445 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr16:56922540-56923600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr16:56922927-56922941 | ACTCCCTGGGGACT | - | 6.06 | EBF1 | MA0154.3 | chr16:56922927-56922941 | ACTCCCTGGGGACT | + | 6.16 |
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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 |
GH16I056888 | chr16 | 56922841 | 56922990 |
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Enhancer Sequence | GCTCACTGCA AGCTCCGCCT CCCGGGTTCA CGCCATTCTC CTGCCTCAGC CTCTTGAGTA 60 GCTGGGACTA CAGGCGCCCG CCACCACGCC CGGCTAATTT TTTGTATTTT TAGTAGAGAC 120 GGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG ACCTCGTGAT CCGCCCACCT 180 CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TCAGCCACCG TGCCCGGCCA CCAGATCTTT 240 TAATTTTTCA GAGTAACTGC AAATGTGAGT TTTTAGGTGA GAACCTCATG CCTCCCTGTG 300 GGCTCCAGAA GGTGCACAGG GAACCAGCTC AAGAGCTCTG AGGCGGTGCC CCTGAACAGG 360 GAAGTGAAAC CAGGACCTGA GGACGGAACT CCCTGGGGAC TTCAGGGCTG ACTCCAAACT 420 CTTCATCAGT GCTTGCTGTG TGATGTCCAG AGATGCCTCC CTCAGTGGCT TTTCTGTGTT 480 GATGTTGTTG TGTGAGGTAT CACTGAACAA CATGAGGCTG AGGGTTGGGG CCCTGAGACC 540 TGCTTCCAGG TATGCTGTTA ACCAGCTGTA GGACTCGGAG CAATCCTCTC AGCAGGTGCT 600 AACAGAATTA CAGCAGCAAC TGATAGAATA CCTGATCTCC AGCCTCCCTC CAGCTCCAAC 660 ATTCCAAACC TTCAAAAAGC AGGGCCTGAA AGTTCCTTGT CCTGGAGATA TGTGATCTAA 720 GGAGCCCAGG GAGGGCAGTG CGCAGCCCAT TGGCCCAAAC CCCAGTGGTG GGCGGGCTCT 780 TGGGCACTGT GTCAATCAGG CAGTACATAC ACCTTTGGAA CAAGAGTCTT CCAGACATCT 840 TTAATTATTT TATTTTATTT ATTTTTGAGA CAGAGTCTTG TTCTGTCGCC CCGGCTGGAG 900 TGCAATGGTG CGATCTTGGC TCACCACAAC CTCTGCCTCC CAGGTTCAAG CAATTCTCCC 960 TCAGTCTCCC AAGTAGCTGT GATTACAGGT GCCCACCACC ACGCCCGGCT AATTTTTGTA 1020 CGTTTTAGTA GAAATGGGGT TTTGCCATGT TGGCCAGGCT 1060
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