Tag | Content |
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EnhancerAtlas ID | HS109-05729 | Organism | Homo sapiens | Tissue/cell | Kasumi-1 | Coordinate | chr12:77313270-77314700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:77314242-77314260 | GAAAGAGAGGAAGGAAGT | + | 6.37 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH12I076920 | chr12 | 77313937 | 77315013 |
| Enhancer Sequence | ACTTTTATTT TGTAATAATT TACTGTCGAA ATTTACTGCC TGAGTGCCCG CAATTATAGT 60 CCCAGCGCTC TAGGTAGAGG GAGAGTTAAT ATTTGTGCAG ATGTGGCAAG GACAGGCTCT 120 GGAGACACAG GGCAAGCTGG CTTTCCTCTG CAGGTGCTGC ATTTATACAG AGCCCATTCT 180 CTCTCCTGTA TCTGCTGCCA TTTCTCCTGC TCCACTACTT CTGCTGCTGC TGTCACTGTT 240 GCTATTGTCA ATCTTGGGCC AGGTCCCAGC TCGGTTGTCC CCACAAGCCC CCTGGACTTC 300 CCAGAGGGAC TGCCGTGCAT GCCTGCTGCC CGCCGGGCTG GTGGTGGTGA GCCCTTTGTG 360 GATGGGCTGC TGGACCACAA CAGGTTGCAT GCAAAGTGGT CCAGCATCTA GCCTCTAGTT 420 ATGCGCATGT GTCACTGTCC CCTCAGCCTT CACCACAGAA CACAAGTTCA AAGATAAAAT 480 AGTAAGAGTT TTAAGACACC AGGACAGAGC ATTAAGCCAA GTGCAGGCCT TGCGCAAATG 540 CAGACTACAA GCCCTTGAAG CCAGTTCTGA TCATTATGCC TTTCTGAGCA ATTACTCCAC 600 CCTGAAATCA GAGATTACTG CAAGACAGTT AGAACTTGTC AGTCTCCATT GTTCTGCCTA 660 GCTTTATGAC ACTGTCCAAT ATCAACCTCA CCCATTCTTT TCTCCAGACT TGCTCCAACA 720 GGGCTTATTG CCCTCACTCT TGCATACTAC CTACCCTTGC TTACCTACTG TTAGTCCATT 780 TGCATTGCTA TTAAAGGAGT ACCCGAGGCT GAATAATTTG TAAGGAAAAG AAGTTTATTT 840 TAGCTCACGG TTCTCCAGGC TGCACAGGAA GCATGGTGAT GGCATCTGCT TCTGGTGGGG 900 GCCCCAGGAT ACTTACCATA ACAGCAGAAG ATGAAGGGGA GCCAGCGTGT GACATGGCCA 960 GAGACAGAGC AAGAAAGAGA GGAAGGAAGT GCCAGGCTCT TTTAAACAGT CAGATCTCAC 1020 ATGAACTCAT AGAGTGAGAA CTCACTCATT ACCACAAGGA AAGCACCAAG TCATTCGCAA 1080 GTGATCCATC CCCATGACCA AAACACCTCC TACTAGGCCC ACCTCCAACA CTGGCGGTCA 1140 CATTTCAACA CATGATTTGG AGGAGACAAA ATACCCAAAC CATGTCACCT ACTAACACTG 1200 TGCCCCCTTT AACAGTTACT GCCTTCCTCC CTTGTCCCTT TCAGTAACAT TTGTTTATTT 1260 CACTGCTTTT TGTCTTTCAC TCCTACCTCA TTCCTGATGC CTGGGGTCAG TTTGCAAATA 1320 AACTACCTGC ATGCCTGCCT TTGTCTCAGG CTCTGCTTTC AGGAGAACCC GGATCCTAAT 1380 AGTTGGTACA ATGCTTGGAG ATGTGATTTT GGATGGGACT ACTTTTGCTC 1430
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