Tag | Content |
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EnhancerAtlas ID | HS182-19507 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr7:2089860-2091250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr7:2090537-2090549 | GCTATTTTTAGT | - | 6.18 | MEF2B | MA0660.1 | chr7:2090537-2090549 | GCTATTTTTAGT | - | 6.62 | MEF2C | MA0497.1 | chr7:2090536-2090551 | AGCTATTTTTAGTAG | - | 6.15 | SCRT1 | MA0743.1 | chr7:2089885-2089900 | TTCCACCTGTTGCAC | - | 7.02 | SCRT2 | MA0744.1 | chr7:2089887-2089900 | CCACCTGTTGCAC | - | 7.52 | TBX20 | MA0689.1 | chr7:2090202-2090213 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr7:2090203-2090213 | TTCACACCTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGCATCTGC GGGCATCACC GCCCCTTCCA CCTGTTGCAC TCCTACGAGA GCTAAGCCAG 60 GTATGAGGCC AGACCAGAAA CCAGAGACCA GGATGGAACC TCACGCGCCT GCTGGAAGCA 120 GGGAATCCCC TAGCCAGTGC CTCAGACCCA TGTCCACACC CACACGGGCA GACGGAAGCA 180 CCAGGCTGAG GGTGGTGAGC CAGGGGGTTC CTGGGCCGCC TCCACTCTGG CTGGTGTCAG 240 GCTGTGGCTT GACCTTTCTG GCAGCTCCGT TGAAGCACCC ACAGAACCAT GGAGACCACA 300 AGCCAACAGT GGCCTATCAC CGGCCTGGAG AAAGTCCAGA CACTTCACAC CTTCTGACTG 360 AGGCCAGGGA CCTCTCCCAG GACCATGGAC ACAGGGACCC AGGCACCCAC CCAGACTGTG 420 GTGCAGGGAA CTTACAAGGC TCTTGGGTGT GCCGTGACAC CAAGGACAAC TGAAGGGGCA 480 GAGGCTGCGG AGGGAGCAGC CCAGTACCCC CGAGGGCGGC TCAGTCCTCA GCAGGCCCAC 540 CCACCTGTGC CTCACAGGCC AGGAGCAAAC ACACCTGTGC GGAACGGCCA GGTGAGGCTG 600 GCTGTCACCT TTAACATCTC TGAATGTCTC CAGGAGGGGC CTAGAGAGGG TTCAGACACC 660 ACCACCAGGA TGCTGCAGCT ATTTTTAGTA GAAAGACTCA AGAGGCTTCC TTGGCAGGGA 720 ACCATGCCTT TGAGCATGAC CATCAATTTT CACCTGCAGC TAACTTCCTT TCCTTTCAAG 780 ATCAAGGTTA TTCAAAGATT TGGATTTCTT CGAAACTGAG TTTAAAGAGA GCATGTTTCT 840 CTACCAAACA GGATAGGGGA TTTTAAAGCA CAAACAAGGA CAATGTCAGG CCAAAGCCTG 900 GGTAGGCAGG ACAAGGTTCC GGGCCTGGTC CCTCCAGCCC TTCCCAGACA CCCTGCAGGC 960 CCTGCTTGTG TCCCCCCGAG GCTGGGCTAA AGCCACCTGT GCCAGCTGGA TGATGCCTGG 1020 CCTGGGCACT GGAGGAGCCT CCCTGGGCTC CTCTCTAAGC CTCGGTCTCT CTGGTATAAA 1080 CCTCCAAAGC TGAGGGGGAC TGGGAATTCC ACAGCCTCTC TCCTAGCAGG ACACTCCAGG 1140 TTTCTCGTCC ATAACCCACG TGGTGCTGTG GAGCCTTGGC CTACAGGACA GAAGGGGCTC 1200 CTGGGATCTG GATGAAGTGG TGGCGAGGGG GGCGCTGACC TTGTCCTTCA GGAAGAGCCA 1260 CGTGGCTCAG CAGGCAAGAT CCAAGACGTT TCAACGTGGT ATGTTAGAAA CTCACACTTA 1320 ATGCAGAAAA GCCCAGGAAC GAGACATTGA AACCGCACAT GAAGACTGGG CCTTCCCTGC 1380 ATCCGCCGGG 1390
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