Tag | Content |
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EnhancerAtlas ID | HS136-13525 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:52208380-52209760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr3:52209232-52209243 | CCACACCCTGC | + | 6.62 | ZNF263 | MA0528.1 | chr3:52208934-52208955 | TCCTTCGCCTCCCCTTCCTCA | - | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 52209020 | 52209193 | chr3 | 52209021 | 52209264 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I052175 | chr3 | 52209021 | 52209264 |
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Enhancer Sequence | CCTGCCTCAC CCTCCCAAGT TATCTGGGAC TACAGGTATA TGCCATTGCA CCAGGCACAA 60 CAGCCTCTTT TTAATATCAA ATTAATGTTT TAATGATGGA CTAGTTAACT CCAAGTTAGG 120 CTGATACTCA GGAACATGCA CTATTTATGC TTTTATGGTT TCATGTCCTC CTCTCCATGA 180 GTTTGAGAAG CAGGGTCACA GCTGGTCATT AAATGGGGCA AGCCAGTCAG GTCCAGGCCC 240 ATAGGGGGCT TTGAGCACAG GGTTTCCAGA ATCTAGGGAA GAGCTGGTAT AAATGCCCAT 300 TGCCAGGCCT GTCAGAGTCT GATTTGGTGG GTATGGGTGG GGCCAGGAGT CTGTATTTGT 360 AACATGTCCC TTCAGTGAAA AAAACAGCTC TGCCTTGCCC TCAAGGAGCA AGGGGACTGT 420 CACCTGGCTA TGATGCCCTG GCCAGGGACA CAAGACTAGA CAAGTCCCAA CTCTGACCCC 480 AGCTTGCTGG AGCCCTTCTG GTTTCAATGA ATGGATGTGG TTAGGGGCCT CCCTGGAGGA 540 AGCGCCTGGA GGCCTCCTTC GCCTCCCCTT CCTCATCATG GCACACTGGC CTCCTCACTG 600 CCCTCCCACA AGCCAAGCTC AGGCCCTCCT CAGGGCCTTT GCACAGCTAT TCCCTCTGCT 660 TGGGCTGCTC ATCCGCCGTG TCATCATTCT GCTGGCTCAT GATATTTCAG GCCTCAGCCT 720 GAACGTCACC TCAGAGTCGC ATCCTCTGAC CCCGCCCCAG CACCCTCTCA TGCCTCTCTG 780 CTCCTCACTC CTGACATGTT GTGAGTTTAT CATTCATTTC CCCTATGACT ATGAGCTCCC 840 TGAAAGCAGG GACCACACCC TGCTGGTCAC CGGTGAATGT GGAACACTTG GCCCTGGCCT 900 GGCACGAAGA AAGATCACTC AGATTTGTCT GATGAATCAA TCCCCAAAAC CAGTGAGCCT 960 GAGTGCACCA GGGAATCCCT CCCACCATCT CCAGCGATGC TTCCACTCAG GGACTTTCTG 1020 TAGGGTGAAG AACAGGGGAT TCAATTCCAC AAGTGTTCGG GGAATGCCAG CTGTGTGCCG 1080 GGGCCTGTGG TGGGGTCACC AGGCTCTAAT GGAGTGGCAG GTGTATACCA GCCCCTGAGC 1140 CTGCCTCAGC GGGAGAAGCA GGTGACTAGC ACCAGAGTCC TTGCTCCAAG GAAGCCAGAG 1200 AGGAAAAGGA CCACCAAGCA GGTTGAGCTC AGGGAGTGTC CTCACGGGGG TTCAAGCCCA 1260 GCACCAGGGG TGCCCCTCGG GTGGCAGGAT CAGGGGTTTC TGAGAAGAGG AGGAGAAAGC 1320 ATTTGGTGTG TTGAGGGGGT ATTGAAAGAC AAGCAGGTAT TCCACAGTGA CGTGGGTGCC 1380
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