Tag | Content |
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EnhancerAtlas ID | HS176-23446 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:241308200-241310040 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr2:241308258-241308269 | ATTGCACAACA | + | 6.14 | MEF2C | MA0497.1 | chr2:241309646-241309661 | GATCCAAAAATAGCC | + | 6.63 | RREB1 | MA0073.1 | chr2:241308846-241308866 | CCCCCACCCGCCCCCCCACC | + | 6.95 | ZEB1 | MA0103.3 | chr2:241308709-241308720 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr2:241308709-241308730 | CCCACCTGCCCTTCCTGCTTC | - | 6.45 | Zfx | MA0146.2 | chr2:241309926-241309940 | CAGGCCTGGGCCAC | - | 6.15 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_37774 | chr2:241308078-241311732 | HSMMtube | SE_52304 | chr2:241308606-241310957 | Skeletal_Muscle_Myoblast | SE_64063 | chr2:241308558-241311158 | HSMM |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I240368 | chr2 | 241307753 | 241314834 |
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Enhancer Sequence | GGGGCACGAG AGGACAGGCC TGTTTCCCCT GCAGCGAGCA TTCTCTGTCC CCCACTGCAT 60 TGCACAACAG GCTGGGCACA GGCAACCCTG GCTGCTCTCT GGCTCCGTGC CTGGCAAGGC 120 CCATCACCTT GTGCCCAGGG TCAGGCCACT CCACGGGCAG AGTCTGAGCT GCTCTCAGCA 180 TTGTCTTGGG GCCAACTCCT GGTGTCAGGT GTCTCCCGGA CCTAGGCTGG AACGTGGGGC 240 CACTCAGGCG TCTCTGACAG GTAGGATCCA GGCACAGGTG GCTCACGATT GATCGACCGT 300 GTGGGGGTTA AATGTCTCCC TAATAAGCCC TCCCACACCT CCTTTCCAGC AGCTGCTAAA 360 TGCCCTCAGG GCACCTCATC TGCACAAATT AAAGTCTCCT GACCCTTGTC TGTGCAACCA 420 AACTTCCTGA AGGCAGCTTC TGTCTCGTGT CTGCTCAGAA CACCACAGCG GGTCCCACCG 480 CCGTGATGCT AAGAGTCATC TGACCTGTCC CCACCTGCCC TTCCTGCTTC ACCTGCCCCA 540 CCCACGCTTG CATCCCCCAT TCACCTGGTC CTGAAGCTGG GAACCCACCT CCCTACACTC 600 AGCCCAACAA AGAGCAGCCA TCCCCAAGCC CTGAGTGACT ATGGCCCCCC CACCCGCCCC 660 CCCACCCACA TCTGGTTCTG CAGAGAGCTG CATGCCTCCA GGTCAGGGCT GCCTGCTCCA 720 AGGTCACCGG TACCCAGTCC AAGGTCGGGG GCATCCTATC TAAGGTCGGG GGACCACATG 780 CCTGCAGGTC AGGGCTGCCT GCACCAAGGT CAGGGCTGCC TGTTTGAAGT TGGAACCAGA 840 CCTGATTTAC CAACACTGTG CCCAGTCAGG GCCTGGACAC AGCAGGTTTT AATATCTGTC 900 CAAGGAATGA AGGCAGAAGT AAAGGAAGCC TTCTCCATTC TTTCAGCAGC CTTGGACGTA 960 CACTGGGCAG GGCGAGGGAC ACTGGGCATG CTTTTCTGAG CAGCAAGGAC TGGAGTCCCC 1020 GACCAACAAC CTCAGGGACC AGCCTCAGGG CATGGGAGGA CTTGAGGGAG GAGGACCCTG 1080 GGAAAACCTT CCAGAGCCCT CTCTGCCAGA GAGAGGTGTG CCTTGCCCAA GATCACTTAT 1140 CCTGGAGGGA CACGAGCTGA CACAGACACG GCCCAGGACA ACCCTGGCAG CCTCTCGCCT 1200 CCTGGACTCC CTGAGTCTCC AGCTTTGCCG TGATGCCAGG GTCCCGGTCC AAGGCCAGCC 1260 TCCTCTCAGC CAGGCAGCCC ACCCCAGCCC AGCCAGGACC AGCTGTGTCT GGGGGAGGAG 1320 GGTGGCCCTG CGGTGGGGGC TGTGGGGAAG GGGCAGATGT ATGACAAGAG GGGCATTGTC 1380 CACACTCCTG ACCAGACTTC CAGGAGCTCC AGGGGCGGGA GCAGCAAGGC AGGCTCTGAG 1440 CTGCAGGATC CAAAAATAGC CTGGGGTGCG GCCAGTGGCC AGGGTTGGGC AGCTGACTTC 1500 ACGCCACAAG CATCCCGGGA AGGCTCAGCT GTCTGTGGCC GCACCTGCTG GGCCTCTACC 1560 CGGAATGCTG CCCTCAGCGG GATGGGCCTG TAACGGGCCC CTGGGCCACC CACATGCAGA 1620 AAGCCCAGCT CCTCCTGAGG CCCCAGAAGC ACCCTCGGGT GCCTGGAGGC TGCTGTGTTT 1680 CTCGCCCTGA CTTGTCCATG GACCCTGGGA CAGCCACGGC CCTCACCAGG CCTGGGCCAC 1740 TTTGCAAGCT GTGGGGGGTG CTGTCTCCCC ATTGAGAGTC CCTGGAGATT TGCCCCACGG 1800 GTTGGGGAAT GACAGCATGA CCCCCACCTA CACAAGGCAG 1840
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