Tag | Content |
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EnhancerAtlas ID | HS061-18942 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr4:84138310-84139430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr4:84138913-84138934 | AAACAAGAAGTGAAAGAAACA | - | 6.05 | TBX21 | MA0690.1 | chr4:84139284-84139294 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr4:84139284-84139295 | AAGGTGTGAAA | + | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_10054 | chr4:84136989-84141360 | CD14 | SE_10843 | chr4:84137802-84141585 | CD19_Primary | SE_11554 | chr4:84130861-84147337 | CD20 | SE_43772 | chr4:84137847-84144361 | MM1S | SE_63025 | chr4:84132108-84203641 | Tonsil | SE_67400 | chr4:84137847-84144361 | MM1S |
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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 |
GH04I083215 | chr4 | 84136970 | 84141673 |
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Enhancer Sequence | CCTGCCCCTT TCTCCCCCTG AAAGGCGTGT GTCCCCTCTC TGTACCTCGC TGGAAGCCCA 60 GCCGCTGGCG CAGCACGTGT TCCTGGCATA CCAGGCTCAC GTGCATGTTA GTGAGCCACA 120 AGATGCAGGG ATGGAGAAGA AAGCCTTCGC CTACCAGTAG CTGCCTGCTA GGCACCAGGG 180 GATGGGCTGA TTTGCTCCAG AATGAATCCA CATCAGGAAT AGCAGTTACA ATTGAGGCCG 240 CCACCTGATT AAGTCTGTAG TAATCTCTCA TTCTCCAGAT CTGCCTGTCT TCTGCAAAGG 300 CCAAACAGGC CAAGTGAGGA CACCTTGAGA TGGTGGACCC CCGCCAGCTG GGAAGAGGAC 360 CCTCACCTGA CCATGCTGAT GCTCTGATTG CAGACTTCCA ACCTCCAGAA CTGTGAGAAA 420 ATAAATATTT GTTGCTTAAA CCACACACAA AATGGGCTAA GATGGTGAAT TTTATGTATA 480 TTTTCCCACA GATACACACA TACACACAAG ATATACTTGA ACAACACCCG CGGGGATTCT 540 GATTAATCTG GGGCTTGGGA AAATGCATTT CAAATATGCG ACTGAGGTGG TTTTGATAGG 600 GGTAAACAAG AAGTGAAAGA AACAGGAAGA TGAACTGTTA CCCGTAATGT GAGAAACCTA 660 TGAGGAAGCT GAACCACCCT GTGGGGTTCT GTCACTGGGA GTGACTTCCT GGTGTTCTGC 720 TGAGCTACTC ATTTTTCACT GTTTTGGTTA TTGAGGTTGA ACTGCTTGAA TGAAAGGTGC 780 GATACTGGGC TCTGGGTGGG GAGAGCAAAA TCTGTTAATC TCAGGGGAGA TGATCAAATA 840 CAAGAAGTGC AGAACTGAAG CTCTCAAAGG GACCTTGGTA ACTTCTAGCA GCTCAGCTCT 900 CCACTTCCTC CTCTGTGCAG TGGGAAAATG AAGCCCAGTT TACGTGTTGT TATTATAGAG 960 ACCAAATGAG ATAAAAGGTG TGAAAGTGTT TTTTACTTTT TAATCAATTA CTCAGTTTAC 1020 TCATAGGGTG AGTGCTTAAA TATGGGCTCC ATAAAGGGTC AGGGCAAAAG TTCTCAACCC 1080 CGAGTACATA TTAACATTAC TTGAGGAGCT TTGAAAAATA 1120
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