Tag | Content |
---|
EnhancerAtlas ID | HS007-11790 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr3:133674040-133676510 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr3:133676001-133676013 | GCTGACGTCACC | + | 6.14 | CREB1 | MA0018.3 | chr3:133676001-133676013 | GCTGACGTCACC | - | 6.14 | ESR1 | MA0112.3 | chr3:133675367-133675384 | AGGGTCATCTAGACCTT | - | 6.06 | TBX21 | MA0690.1 | chr3:133674228-133674238 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr3:133674228-133674239 | AAGGTGTGAAA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAACGAGAGT GCTTGCTGGT CTCCACCACC CTGGTCTCCT GGTTCCACCG GCTGGCCTCC 60 AAACCCGGCC TTTCTCCCAG GCCCCTTGGG GAAGGACCAA CTTTGGCCAG AGGCTGTGCT 120 AGCAAATGGG ACATGGTTCC TGAGGACCGC GTCCTTCTGT CTGGCCAGCA GGAGGGACTC 180 TAGAAACAAA GGTGTGAAAG AGAGGTGGAA TGTGGGCTCC CCGGCCCCAG GAGCTGCTAT 240 TTCTCAGGTG GAGAGGAATC TTCCTCTCGT GAGTGTCCAT GCCTTCTCCT CCATGGGCAC 300 TGGTGGGGAG CTGAGCACGG AGAAGTCAGT ACCTTCATCT GTGGAGGAAA GGGGCACCCA 360 GCTGGAAAAG GGGGAGGGGG TCCAGGGTCA AAGCCCAGGC CCGTCGGCCT CCAGCACCCT 420 GTGCTCAGCC CTGGGGCTCT GGGCCCCCAG GGTTCTCTTC AGCAGGACAG AGGTCATGCT 480 GTTGCACCGG GTTGGTGTCA CCTACAACGT GGGTTGAGTC CCTGGTTGTG ACTCCCAGGG 540 CCTTTGCTTC TTAGTGAGCC CAGCTCCAAG TCACACTGGA AGACCTACTG CCAAAGACAT 600 TTAATATCCT TACCGTTCCG GGGAAGCTCC CAGAACTTCT GATGCTGGAG GGGCTTTAAG 660 ACCCTCTCGT TCAGCCTCTC ATATTACAGA TGGGGAAGCT GAGGCTGCTT CTCGAAGCCC 720 TTCTGTGAGG GTCCCAGACA CCCTGGGTGA GGCCTGTGGG CACTATGGTT CCTGTGGCTG 780 TGGCCCTTGC CAGGCTGGGC TGCCGCTTCC ATGCCTCTGT TTTTAATTTG GCCCACACTA 840 AGCAATCAGC ATTGGCAGCT CTCCAAGGCC TTAGGGGTTC TCGAGGGCTC CTTTCCATGA 900 GATCCCCTTT CCCTGTCTCA TTCAGGCTAA TGGAAACCAC TGACGTCACC AATCTCACTC 960 GCTTAACACT AATGGGATTC CGTTTAATTC TCACTTGTGC TGCCCTGAGC TAGGTGAGCC 1020 TAAGTCCCAC AGAGAGGAAA ACCGAGCGCC GTAGACTAGC CCTGCTCCTC ACACTGGACT 1080 CTGCCGGTGC TGTTGGGCTC AGGGCTGCCC TGGATGGTGG GGCTGGGGAG AGGGGTCTGT 1140 GCTCTTCATT GCCCTTTCCC CTCTCCCCAG TCGCACACGC CTCGTCCAGC CTGGCCCCAC 1200 TGTTGTCTGC CCTCTCCAGT GGTGTCTATG CAGGACACAT TAGAAAGTTG CTGTCATGGG 1260 AGCTCCCCCA TCAGTCAGGG AAGCCTGTCC CAGGAAAAGG AAAGGAAGCC AAGGCGTCTG 1320 TTTGGTCAGG GTCATCTAGA CCTTCAATAG TTGTGTCCGT GGAAGGAAGC ATCCTGGCAA 1380 GCAGCCAGGG ACTGTAGTCA GGGTCCCTCT GTACCTCCCT CTTCCCACTC CATGTTCATT 1440 ATCCTGCCTT TCAATGCAGA ATTCAAATAG AGTGGCCCGA CCACATGGTG ATATAATATG 1500 CAACCTTTTA GAATTGGGGT GAAAATATAG CCTTTTTTTT ACACAGAAAG ACAGCTGGAA 1560 CAGCTTGTTA GAATAAAAAA ATAGTAACTA GTAGCTTGGA GAAGAATATG TTCCCTAATT 1620 TATAAAACGT TTGTGGACTA CTTGAATATG CAGAGAAAAC CTCTGGAAGA TGATGGCTCT 1680 CTCTGGGTGA TGAGATTGTG CTGATCTTTT TTTATTTGCC TCATTTATTT TGTAATTTGT 1740 CTGGAATGAA CACATTTCTT TTGTGTTAAA AGAAATACTT TTGAAATAAA GCAACAAAGT 1800 TTTTAAATTC AAGGTTTTTG TAAATAAATA TATCCAAAGC TTAACAACGT CTCTCCCATT 1860 TCTTCTTTGT CCCATTCCCA TTGCCCTTCT TTCTGCTCTA GGCTCTAGGC CTGCAACAGT 1920 GGAGCTGAGT CTCTGCCCAT CCCCACCAAC CACAACCCAT CGCTGACGTC ACCGATCTTG 1980 CTCACTTAAC ACTGATGGGA TTCAGTTTAA TTCTCACTTG TGCTGCCCTG AGCTAGGTGA 2040 GCCTAAGTCC CACCAGAGCC CACCACCACC TCTCCCCCGT GGAGTGTTGG GCCTCTCTCT 2100 GATTTACAGG CTCTACCGTA GAGATCCAAG TCCTAGCACC AGAAATGTCA AACACCCATG 2160 TACTGACAGG GCCAGGCCCT GTGCCAAGGT TGTGATGTAT GTGGTCTCCT GCTCACAGGG 2220 GTTACTGTGA GCAGGAGACT ACATAAGACC ATACCTAAGT AGCTGGTTTG GGGGTAGAGC 2280 TGGGATCCGA ACCTGCATGT GTCTGACTCA AAGTCCAAAC TGAAATCAAG TCTGATGGCA 2340 GCTTGAAAAG ACAGAACACA CATTTTTCAG GGATGGAAGA ACATGGCATG GGAAGATTTC 2400 CTCCATCCCT AGCCACCTTC AGACATATGA GCTCTCTGAC CTCTGTAGGT GGCTGGGACC 2460 TTACACCTAC 2470
|
| |
|
|
|