Tag | Content |
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EnhancerAtlas ID | HS110-03116 | Organism | Homo sapiens | Tissue/cell | KATO3 | Coordinate | chr20:60551430-60552810 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:60552550-60552568 | CATGCCGTCCTTCCTCCC | - | 6.17 | HES2 | MA0616.2 | chr20:60552325-60552335 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr20:60552325-60552335 | GGCACGTGCC | - | 6.02 | KLF5 | MA0599.1 | chr20:60552539-60552549 | GCCCCGCCCC | + | 6.02 | REST | MA0138.2 | chr20:60551538-60551559 | GGTGCTGTCCAGGGCCCTGCC | - | 6.61 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAGAGTGGG GCTTGCAATG AGCCTGTGTA TCTGAGCCAA GTACCCCGAT TCCAGAGGAG 60 GCCAGGCCTG GCACGGGCTC CTTCCGGTAG GCCCACAGCT GGAGCTGGGG TGCTGTCCAG 120 GGCCCTGCCA GGGCAGGGGC AAGGGCAGGA GGCCCCATGC TGCACCTTCA GGACAGGGCA 180 CACTCAGATG CTGCCCAATG CCCCACAGTG CTTGGACCTG GTCCTGGGGC TGAGGATGGA 240 CTAGGGGGTG GCACCCACCC AAGGCAAATG GCTGAGCGGC CCCAGGGCCA CCCTCCATGT 300 GACCACAGCT GGACTGCCTG TGGACTCAGC TGGGGCACAA AAGCCACACT AGGTCTGTGT 360 GTGTCATCCC CGCTTGGCTG CTGAATTCCT GCACTGGGAG GCCTGGGGTT GGCTGGGACT 420 GGGCATGCTG GGTCAGCTGG GAAGGCTGGG TTTCTCAGTG GCTCCCACAG TGATCCCTGA 480 GCCTCTGGCT GGGCCCTGGC TGCACAGACG CCGCCTCCGT CAGCCCCTAC AGGTGACCAG 540 GTGTCTCCCG AGCTGCCTCA GATGTGTTCC TGCTTGGAGA AGCATAGCTG CTGCGTGCCA 600 GCTCCTGTGG AGAGCTCTGG CGGTTTCAGC TGATGACACC TGCATGACAC CGCCCAGCAG 660 GGCACGCGCC ACACACACGA CACCGCCCAG CGGGGCACAC GCCACACACA CGACACCGCC 720 CAGCGGGGCA CGCGCCACAC ACACGACACC GCCCAGCGGG GCACGCGCCA CACACACGAC 780 ACCGCCCAGC GGGGCACGAG CCACACACAC GACACCGCCC AGCGGGGCGC GCGCCACACA 840 CACACAACAC CGCCCAGCGG GGCGCGCACC ACACACACAC GACACCGCCC AGCGGGGCAC 900 GTGCCACACA ACTCCCAACA GCTGTCATTT CCCCCAGCTG GCATGAAAAC TAAGTTCTGC 960 TCCGATGGTG AAAGCTGCTC ACATATATTT AAGTACAAAG ATTACGATGG CATCTTTACA 1020 GCACATTCTC AACCAAAGTT AAGATGCTGG AAGGAGCGGA TTCTGCTGTG TGTGCCAGTG 1080 GGAGCCTTGC TGTGAACAGC CCTGACATGG CCCCGCCCCT CATGCCGTCC TTCCTCCCCC 1140 CTTCCCCGTT CTGCCACTTT CAGTTCAGGC TGGGAGCATG GCTGCCTTGT GTGATGGCAT 1200 GCAAGTGTGT CTCTGACCCA CTGCATTTTC TTTATTCCTG TGAGATTCAA ACAGATGAGG 1260 GCACCTGTCT CCGTTCAGAC GCCCTGCGCT GTGAGGGCCC TTCTTCAGAC CTGCCCGGGG 1320 TCCCTTTGCT ACTGAAGCCT CCGCACTCCA CACTAGCTCA TTATAAAGTG ATCCGCACCT 1380
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