Tag | Content |
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EnhancerAtlas ID | HS098-58920 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:132372010-132373840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr9:132372573-132372584 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr9:132372573-132372583 | GCCCCGCCCC | + | 6.02 | Klf1 | MA0493.1 | chr9:132372276-132372287 | TGGGTGTGGCC | - | 6.62 | SP1 | MA0079.4 | chr9:132372570-132372585 | CAGGCCCCGCCCCCC | + | 6.65 | SP3 | MA0746.2 | chr9:132372572-132372585 | GGCCCCGCCCCCC | + | 6.11 | SP4 | MA0685.1 | chr9:132372570-132372587 | CAGGCCCCGCCCCCCCC | + | 6.76 | ZNF263 | MA0528.1 | chr9:132372463-132372484 | GGAGGGGGGAGGAGGGGGGGA | + | 6.19 | ZNF263 | MA0528.1 | chr9:132372488-132372509 | GGAGGGGGAGGGGAAAGGGGG | + | 6.23 | ZNF263 | MA0528.1 | chr9:132372508-132372529 | GAGGGAGAGGGGAAAGGGGGG | + | 6.66 | ZNF263 | MA0528.1 | chr9:132372460-132372481 | AGGGGAGGGGGGAGGAGGGGG | + | 7.01 | ZNF263 | MA0528.1 | chr9:132372491-132372512 | GGGGGAGGGGAAAGGGGGAGG | + | 7.47 | ZNF263 | MA0528.1 | chr9:132372485-132372506 | GAGGGAGGGGGAGGGGAAAGG | + | 7.52 | ZNF263 | MA0528.1 | chr9:132372504-132372525 | GGGGGAGGGAGAGGGGAAAGG | + | 7.84 | ZNF263 | MA0528.1 | chr9:132372467-132372488 | GGGGGAGGAGGGGGGGAGGAG | + | 7.87 | ZNF263 | MA0528.1 | chr9:132372478-132372499 | GGGGGAGGAGGGAGGGGGAGG | + | 8.46 | ZNF263 | MA0528.1 | chr9:132372470-132372491 | GGAGGAGGGGGGGAGGAGGGA | + | 8.72 | ZNF263 | MA0528.1 | chr9:132372481-132372502 | GGAGGAGGGAGGGGGAGGGGA | + | 9.38 | ZNF740 | MA0753.2 | chr9:132372578-132372591 | GCCCCCCCCCCAC | + | 6.29 | ZNF740 | MA0753.2 | chr9:132372576-132372589 | CCGCCCCCCCCCC | + | 6.64 | Zfx | MA0146.2 | chr9:132372570-132372584 | CAGGCCCCGCCCCC | - | 6.19 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_32072 | chr9:132370605-132374195 | Gastric | SE_34237 | chr9:132361675-132375787 | HCT-116 | SE_35734 | chr9:132371607-132373414 | HepG2 | SE_54057 | chr9:132368120-132374012 | Spleen | SE_56758 | chr9:132370678-132373789 | VACO_400 | SE_68279 | chr9:132368936-132439405 | TC32 | SE_68280 | chr9:132368936-132439405 | TC32 | SE_68281 | chr9:132368936-132439405 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TCTTCCTCAT CCCCTGTTCA TGGTGGGGGA CATGCTGGTG GACAGACAAG TGGCTACAGA 60 GGGCCAGGGG GAGGCGTCTG GGCCTCCAGG GCAGCAGATG ACCCCGAATG TGGGGGCTGC 120 GGCCCTGGGA GACCCCGTGA GAGGCCGTGT ATGTGTGAGG TCGGCCTGTG TTCACCGGCT 180 GTTTGTAGGG CAGGAGTCCG GGTATGTGTG TGGTGTGTGT GTCTGAAGGG GGTGTCTGTG 240 GGGCGTTGTT TTGTCTGTGT ACCGTGTGGG TGTGGCCCTG TGGTGTGCCT GTGTGTGTCT 300 CGGGGTGCGT ATCTCGGTGG TGGGTGTGAG TGCCGAAAGC GGCGGGACTG AGGCTTCCGT 360 CCTCCATCTG TGGTCTGCGG GGAGGGAGTG GACAGCGCAG GGAGCGGACA GGAGCGCTGC 420 GGGATCCCGG GGCCTTGCGG GCCGAGCCAC AGGGGAGGGG GGAGGAGGGG GGGAGGAGGG 480 AGGGGGAGGG GAAAGGGGGA GGGAGAGGGG AAAGGGGGGA AGGGGAGGGG TAAGCGGTAG 540 GCGGGGGCCA GGTCTCCCTG CAGGCCCCGC CCCCCCCCCA CCGGCGTGGT GCCCCCGGCG 600 CGAGCAAGGG CGTGGAGTCC GGGGTCGCGG GGGCGCCGAG ACCCGCCCCG GGGGCTCCAC 660 GCGGACTCCG GCTTCAGTGC TCGGCGCTGC CGCACGGCTG CAAGCCTAGC AATTTTGGGC 720 TGAACAACAA AAGCGAGAGA GAGGGAAGTT GGGGGGCGGG GGCGGCGCGT TTCCCCCCAC 780 CCGCCAGGGC CGGTCGTGGG CTCGGAGCAG GTGCCAGGAG GTCGCGCGGC CGGAGCGGGG 840 CTGTGCGGAG CCAGCAGCGC GGAGGCGGAG GCGGGCGGGC GCGAGCGCCG CGCGAGGGGA 900 AAAGTTTCCG ACCCTGGAGC GAGAGGCTGA GAAGTTTCGG CCGCGCCAGG CGGCGCCAAA 960 GCCAGGCCAA CACTGCCCCC GCGTGGGCGC GCCGCGGTGC TGCAGCCGGC GCAGGGGCCG 1020 GGGCCCGCCG CGACCCTTGG GGTAAACTGA GGCTCAGAGA GGGCGACGTG GGCTGCGCAA 1080 GGCCACCTGG AGGAGGGGCC GTAGAATCAG GCCTGCTGAG ACGGGGGACG GGGCGTGAAT 1140 GTCCAGAAAG GGAGACAGAA GGGAGGGGAC GTCCCAGGGA CTGAATCCCA CTCCTCGTCC 1200 TAGATGTGTC TCCACCCCCT TCCTTCCAGT TACCTCCAGA GTCCAGCAAT CAGGTACCCG 1260 GTGGAGGGGC GGTGGCAGTG CTGTCTTCTT CCCATCCCTG CAGAGTTTGT CTAAACTAAC 1320 CCTAGCTCTA TTGCCCTTCT TCTGGAGTTA GGGCGCCTCT CCCAAAAGGC GTCCCCCATC 1380 CACAACCCAT CCCGGCCCTA AGGACCCCCA CCAGCCACCG CCCAGGCCAG TCCCACCGTT 1440 TGCAGCCCAT TCCTTTGCCA TTAAACAAGG CGCCAGGGTG TGGATTCCCT GCTGTTTCCT 1500 CAGCGGCCAG GAGGTGGCGA GAAAGACCCG GATCCTGGGC AATGGCGCGG GTCTGGGGGC 1560 CACTGACAGC TTCAGGGAAA GAGGCGGCGG CTCAAACTTT CTCCAGGGGG CTGGAACGCA 1620 GGTGTGGCAG GGGCAAACCT GGTGGGCAGG GTCTGCCACC TTGTCTTTCG CCACCTCCTG 1680 ATGCAGATTT GAACATCCAC CCCCTCATCC CCAGACTAGG AGAGAAACCG TGGGCCCCAG 1740 CCCGTCCCAC ACAGGTGCTT TGCCTTCTGG GACCAGAGGG TGCCAACCCT TCCGGGGAAA 1800 CGCATGAGAC CAACACAGGG CTCTCTTCCC 1830
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