Tag | Content |
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EnhancerAtlas ID | HS059-09585 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr12:898140-899990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:899947-899965 | CCTTTCTTTTTTCCTTCC | - | 6.5 | EWSR1-FLI1 | MA0149.1 | chr12:899951-899969 | TCTTTTTTCCTTCCTTCC | - | 6.79 | EWSR1-FLI1 | MA0149.1 | chr12:899955-899973 | TTTTCCTTCCTTCCTTTC | - | 7.66 | FOSL1 | MA0477.1 | chr12:899548-899559 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr12:899548-899559 | CATGAGTCACC | - | 6.02 | NFAT5 | MA0606.1 | chr12:898440-898450 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr12:898440-898450 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr12:898440-898450 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_18551 | chr12:896261-899772 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 899072 | 899326 | chr12 | 898377 | 898428 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I000788 | chr12 | 897977 | 899366 |
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Enhancer Sequence | TTTTGTGGGA AGGTTTATTA GTTGGTTCTC AAATGTGAAG GCCACATGCT TCCTTCAATT 60 AAGGCATAAT AATGAAAGGA CATACTGAGG CTACATTACA TCTTTGTTGG TGAAATCAGG 120 AGTAGAGGAA AGGGTAGAAA CTAGAACAGA TACAGATTGG GAAGTGGAGA GGTAAGATTC 180 TTAGCCCATA ATTTTCAGAG AAAGTAGTTG TTTGTTGATG GCACCAAACA GGGCTCCTGA 240 TTTATGATAA AGAATCATAC ATTTGGTAAA AGTTACAGTC TGAAGTACAA AACCCCAATG 300 ATTTTCCATT CTAGTGCTTC AGTGAGAAGC TTAACAGTGT ACTATGTATA GGTAGATAAG 360 AATAAAGTAA AAGACAGAAT TCTTTGCTGT TAAAATGAAA GAATAACTTT TACTTAGCAT 420 AGTATGGTAG TATACTAATA AATGGTACAC ACTGCTAGTC ATAAAATTTA GATTTTGTCC 480 CCAGTTCTAC CTGTATACCT GTATTATTAG TCCTTTGTTC TCTGTTCAGT GTCCTAGTAG 540 AAACTGTGTG GTTATACTCC TTTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCGCTCTGT 600 CACTCAGACT GGAATGCAGT GATTCAATAC TCACTGCAGC CTCAAACTCC TGGGCTCAAG 660 CAGTCCTCCC ACTGAGTAGC TGAGACTACA GGTGTATGCC ACCAAACGCC AGGCTAAGTT 720 TTTTAAAGAA CTTCTGAAAG CATAGAGTTT TCAGGATGTT TTTATAATAT TTCATAGATG 780 GTAAGGCAGT GTCAGATTGA TTCAGTTATG TCATCAAATG TCTCTCTGCC ATTCTCAGCA 840 TGTATTTCAG GCTAATGCCC CTTATGGCCC TATTTTCAGC CATCACATGC ATCCTGGATA 900 GCATTCAGCA GCAGAAGCAG CAATTTCTTT AACAATGCTT CATATCTTAC TGGTCAGAGT 960 TGTGGGTCAC ATGGCTTTGT CTAGATCAAA TACTGAAAAT GGAACTTCCA TGATTGGGTT 1020 AGGCCAGTTA TGACTGTCTT GACAGGAGAT GGGGCTTGCT TTTCCTCTAG TACAAGATAG 1080 ATACTTAAAC CAAATAAAGG ATTATGGTTA GCAAGGAGGA GGGGGTTTGG GAATGACCCA 1140 GTAGTAGACT GCCAACAGTG CCTGCTACTT AACTCACTCT TGCGAGATGG GGAAGTAAGA 1200 TAGTCTTGAG GGTTGGGGCT ATAGTAGAAT AGAAGGAAAT GACTTTTTGG AGAAAGTGAT 1260 TTCTTTTTAT CTTTTCATGT TTTTATTTTT TATTACATTT TGTTTTTTAC TTAGGGATGG 1320 GGTCTTGCTA TGTTGACCAA GCTGATCTCA AACTCCTGGC CTCAAGCCAT CCTGTCATCT 1380 CGGCCTCCCA AAATGGTGGG ATTACAGGCA TGAGTCACCG TGCCACATCT GGAGAAAGTG 1440 GTCTGTAAAC TAAGTTTTGT GGACAAATGG AGATTATTAG GGAGAAAGAC TTTTCCTTAT 1500 CCTTCTGAGC CCTTGGTTGT CTATGGGTAC TGTTGCTTGT TTTCATTTTT AAGGATAGTA 1560 AACATACTTA ACATTTCCCA AGGAATCTGT CTTGACCTGT GTATGTGTGT GTAAAAGCTG 1620 CATTGTGGAC TTTTTGAAAA AGAACATATA ATAACCAGTT CAGTTGAATG CAACGTGCTC 1680 TGTGAGATTA AGGGCTCACA AGAAACTGCT AATCACAGTT TTAAAAAGAC AATCTTTTGA 1740 TGTCTCATAT CTTAGTGTTA CTATGAGTTT ATAGCCTGTT ATTTTGTTTA GTGTTTACTC 1800 TGTCTTGCCT TTCTTTTTTC CTTCCTTCCT TTCCTTTTCT TTCTTTTCTT 1850
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