Tag | Content |
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EnhancerAtlas ID | HS136-05911 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr14:50396030-50397310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:50396928-50396949 | TTTCTGTTTCTTTTTCATTTC | + | 6.6 | MEF2A | MA0052.3 | chr14:50396758-50396770 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr14:50396758-50396770 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr14:50396757-50396772 | TTCTATTTTTAGTAG | - | 6.57 | Nr2f6(var.2) | MA0728.1 | chr14:50397164-50397179 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_62298 | chr14:50396222-50471436 | Tonsil |
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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 |
GH14I049929 | chr14 | 50396515 | 50397409 |
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Enhancer Sequence | ATATATTCAA AGTGTACAAC ACGATGATTT GGTTTGCATA CACATTGTGT AATGATTTTA 60 TTTTTTCTTT TTCATTCACT TATTTCCTGA ACTCCGGCAG CTTACGTTTT ACCTCCTTTG 120 GTCATCTCAC CTTCTCTTCT TCAAGATATT ACTTCTGTTT TATGATTGTT TTGTGGAAAC 180 AATTGCTTCA TTACATTTTT TAAAAAATTT ACAGCAAGAG ACCGGGTGTG GTGGCTCACG 240 CCTGTAATCC CAGCACTTTG GGAGGCTGAG GAGGGCGGAT CACCTGAGGT CAGGAGTTCG 300 AGACCAGCCT GACCAACATG ATGAAACCCC GTTGCTACTA AAAATACAAA AATTAGCTGT 360 GGCACATGCC TGTAATCCCA GCTACTTGGG AGGCTGAGGC AGGAGAATTG CTTGGACCTG 420 AGAGGCAGAG GTTGCAGTGA GCTGAGATTG TGCCATTGCA CTTCAGCCTG GGGAACATGA 480 GCGAGACTCC ATCTCAAAAA AAAAAAAAAA ATTTGCAGCA AAATGTTCAA AATTTTAATC 540 TGCTCTGAGG TAATGTTTTC TTTTCTTTTT TCTTTTTTTT TTTTTTGAGA CGCAGTCTCA 600 TTCTGTCACC CAGGCTGGTG TGTTGTGGCA TGATCTCGGG TTACTGCAAC CTCTGCCTCC 660 TGGGCTCAAG TGATTCTCGT GCCTTAGCCT CCCAAGTAGC TGGGTGTGCC ACCACACCCG 720 CTAATTTTTC TATTTTTAGT AGAGACAGGG TTTCATCATG TTGCTCAGGC TGGTCTCGAA 780 CTCCTAACCT CAGGTGATCC CCCTTCCTCA CCCTCCCAAA GTGCTGGGAT TACAGGCGTG 840 AGCCACTGAG CCTGGCCTGA GGTAATGTTT TCATGGTGAT TATTCATCAG CATTTGTTTT 900 TCTGTTTCTT TTTCATTTCC TTTTTTTTTT TTTGAAGCAG AGTCTCGCTC TGTCACCCAG 960 GCTGGAGTGC AGTGGCACCA TCTCAGCTCA CTGCAATCTC CACCTCCCAG GTTCAAGTGA 1020 TTCTCCTGCC TCAGCCTCCC AAGCAGCTGG GATTACTGGC ACGCACCACC GTGCCCAGCT 1080 ACTTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGTT GGTCAGGCTG GTCTTGAACT 1140 CCTGACCTCA GGTGATCTGC CCACCTTGGC CTCTCAATGT GCTGGGATTA CAGGCGCGAG 1200 CCACTGCACC CGGCCTAATT TTTGTTTTTT TAGTAGAGAC AAGGTTTCAC CATGTTGACC 1260 AGACTGGTCA ACCACTCAAA 1280
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