Tag | Content |
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EnhancerAtlas ID | HS017-06607 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr11:113822200-113823830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr11:113822955-113822966 | TGATTAGATTA | - | 6.32 | Nfe2l2 | MA0150.2 | chr11:113822353-113822368 | CACTGTGACACAGCA | + | 6.09 |
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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 |
GH11I113952 | chr11 | 113822723 | 113823726 |
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Enhancer Sequence | CCTCCCCGAG CCTCTGCAGC CTTGAGTATT GCCAATAATC AGGTGGCAGA GGGTCTCCTT 60 TTCCTCCCAA GATACCCGCC ACACCTTTTG CAGTTGTCCT AGAGGAGCAG TAGCTGCCAT 120 GATAAAGGAA GCTGAGTTTT TCACCTTTTA AACCACTGTG ACACAGCACG TCTCCTGGGG 180 TCTGACGTCC CAGCCTGGAT GAGCCAGAAC CGGGAAGCAA ATGAGAGTGG CCATGAGGGG 240 AGCCAGAGTG AAAGTGCCGT TGCTAGAATG CATCCTCCTC TCAGCTCAGC CTCAAGGCTT 300 CCCCAGATGC TCTCCCTTCT CAGAGATCTA ATGACACATG TTAAGGCAAG GTTAGTAGAA 360 GTGGGTGGAG TCTGAATTTT ATCCTGCCCT GTGGCTCTGA GGCTTCTAGG AAACTTCAGA 420 GCTTGGGTTT TAAGGTAAAA TCCACCAATC AATTCTTGCA TGGTGGATTG TCTCCTCAGG 480 GCAGAGAGCC CTTCGGGAAG GCCGGGCTTC CTTCCTTGCA ACCCCCTCTG TGACCCTGGG 540 CTCCACCTCA GCCATCACCC TGTCGAGCTT AGCCTACCTT GTCCTGTTCC CTCGATCAGA 600 CTCCATCTCA GCAGCCGGAA CTGCTCAGTC CTGACTTATT TACCTGCGGA GACAGTAAGA 660 GCTTCATAAT TAGCTGAGCA ACAGCATGGA GGCTTTTATG AGCAGCCACG CTCCCCCCAC 720 ACTCTGGTGT CCGTAATTGA AATGACCCAC GCCAGTGATT AGATTAGGGG GCTGAAGAAG 780 CCCAGCACGC TGCTCCCCGT CCTGTCGGGG AGGTGATGTA ATTAAGTTTG TGCTTCATTT 840 GGCAGAGGCT ATAAAGCAGG AATTGCATCA AGGTTTTCTG CAGGGGTGGA AGGAACTGCT 900 GGGCTGTGGG CGGCCTCTGT GTCAGGCAAG ACTACAGATC TGAGTGAGAG GGAGCCCCTT 960 GCTCCCCCTT TACCTTACCC TCTGTACCTC TCCCACAGCC TGTGTTGGCC TTTGAAGGCC 1020 TGGGGTGTGT GTAAGTCTAG CGGGAAGGTC ATCCCTCCTC AGTGTCACTG GTAACCCGGG 1080 CTGCATGTGG ACAGCCAGCT CCTGGTCACC CTGCTCATCC TCTTTGAAGA GCGCCAGGCT 1140 GAGAGCAAGG GAATCGGGTG CTGTTGGCAG TTCTTTTTCT CCCCATATCC CTGCCCAGTC 1200 TCGGCTTGCA GCTCTTCCTT CCACAAGCCT CCTTCTCTAC CCCAGCCCCA TTCTCCTGCG 1260 GTCTCTTCCC ACCACCTGCC CTTTTGCACG CGGGGCTGGC TTTGGCCAAG TTGTGCAATA 1320 GCTGAAGTTT CTTCTCATTC CTTCCTCTTT CCCACGCGTA TCTACCCAGG GACCTATGTC 1380 GGCACACTGC CCAAAGGACA TCTCACTGTT GTGTTCTTCC CAAATCTACC TTCCCGGACA 1440 CTGTGCACAA ATGAGACCAA AAATCCTTCC ACTGTGCCAA TGCCTTTTAA ATACAGTCAT 1500 TTAAAATTAA TCTGTTCTGA AATACAAACT GGTGAAATGA GTTCATGCCA CATTTTCAAC 1560 CTGGGGTATA TTATCCCTAG CATGGCTCAG CAGTGTGCTA GCTATACTCA AAACCCCAGA 1620 ATGAACATGA 1630
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