Tag | Content |
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EnhancerAtlas ID | HS121-03955 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr1:227073380-227075790 |
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) |
MEF2C | MA0497.1 | chr1:227073977-227073992 | TTCTATTTTAGGCTC | - | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 227073656 | 227074400 | chr1 | 227074000 | 227074083 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226886 | chr1 | 227073902 | 227074101 |
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Enhancer Sequence | GTGAGGCCCT GGCCCTGCCC TCCAGCCACG CTTCTCTCCG TCTGCCCCAC ACCATGGCGG 60 CAGGGCCCGT GAAACAGCCG CCTTTAGAAA AACACAAATT AGAGGAAAAT AGACCCAGAT 120 TTTTTGTACT CCTCCCCACC CCATCCTGTC TCCCACCGTG GATGACCTAA TACTGTTGTC 180 TTTTATTTTT ATTTATTTTC TTTTTCTTGA AACATGGTCT CACTCCATTG CCCAGGCTGG 240 AGTGCAGTGG TGCGATCATG ACTCACTGCA GCCTCAACCT CCTGGGCTCA AGTTCTCCCA 300 CCCAGCCCCT CAAGTAGCTA GGACTACAGG TTTGCACCAC CATACCTGGC TAATTAAAAA 360 ATTTTTTTTT GTGCAGGCTA GATCTCACAG TGTTGCCCAG GCTGGTCTCA AACTCCTGGA 420 CTCAAGTGAT CTCCCACCTT GGCCTCCCAA AGTTCTGGGA TTACATGTGT GAGCCATTGC 480 ATCCAGCCTG TTGTCTTTTA AATTTACACA TTATCCCACT TGAGTTCCTC ATTGCAGTGT 540 TCCAAGCATC ATTTCTCATA TTTCAAAGTT AATTTTGTTT TGCTTCTCTT TCTGAAGTTC 600 TATTTTAGGC TCCCCTCACC CCGATACTTC CCCTGAAGAT TTATTTTTAG TTTTCCTTTT 660 CCTTTTCGGG CAAGGATGTG CAGAGGCCAT GCTGAGGTCT TGCAGCCCTG GGAGACTTTT 720 GGGTTGTAGC TGCCTATAGC TGCCGAGTAG CCCCAGGGAG TAGTGGAAGG GCAGATCCCA 780 TCTGGCCAGA ATCATGGGCA CTGCCTGTCC CCAAAGATGC CATAAGCTTT TAGACAGCGG 840 CTTCAGGCTT TTCTCCCAGG TAAGGGGTTG AACCCCTAAC GATGGAAAGG AAATTAAGCT 900 GGGCATTACC TATTTTAAAA CTGTTTACAC ACAGGTGCCT CACAGCATTT TTTGTTCAGG 960 CCGCTGCCAT CCATGGAGCA GGTAGATAGA AGTGCAGAGT GCCCAGGCTA GAGGGATGGG 1020 ACAGGGACAG TGCAGGGAGG GAGCTGAGCC CCCTTCCAGC GGGGGCAGCA GAGGGGAAAG 1080 CCATGGGAGG GGCTGCAGGA TGTGTCCTGA GCTGAAGCTT ATCAACAAGT AATGAGTACC 1140 AGCTGGGCAT TGTGGTGCAC GCCTGTGGTC CCAACTACTT GGGAGACTGA GGCAGGAGGA 1200 TCGCCTGACC CCAGGAGTTC AAGTCTAGCC TGGGCAATGT AAGACCCTGT CTCTAAAAAA 1260 ATAATAATAA AATAAGTAAC AATTACCTGT GTAACTGTGA CGAGGCAGGG TTTGAACATT 1320 GCCGCTGGGA GGTTGGCAGA TGGTGGGAAG CAGGGTGGAG GGCTGCTGGT TTGGAGCAGA 1380 GGATACAGAT TGCATGGGGT CAAGCTAGAA ATTGCGTGGC AGATGTGAAG AGCTGGCCCC 1440 ACTGCGGGCA GTAGGTGTCT GGTGGCCAGT CCCAGAGGCT GTGAAGAGGG GCTCAGCCAT 1500 CTGTCTAGTA GGGCTTCCTT GGAGGTTCCA CGATACAGGC AGATGGTGGT GGCCCGGGCA 1560 GCCAGGTGGT GGCTGGGATG AAGAGGGTTG GCAGGTCCCA GAGGCAGCCC CTTCCCCTTT 1620 TGGCTGTGTG TGCAGCAGGG CCGTGGAGGC TGCTTTTAGT CCAGGTAGAC CAGGGCCACG 1680 CTGAGGTCCC AGTGGGCTGA GCTGGTGACT GATGAGTTGG TCCTCAGGGG TGAGGCTGGT 1740 GGGAAGTGAT GTCACTGTCC CGCCGATGGC CAGCTAAGGG ACTGGGTTAG GATCAGCCCC 1800 CTCTTGTCCT TCACTCTCCC ATCCTTGGCC AGGAGAAGAG GAACAGGTCT TTCTGAGGAC 1860 CTGCTTGTAG ACCTTTGGGT AGGAGGGGAC TTCCCAGGTT CTCTGTTGAG GCCACTCTAT 1920 CTAAAATAGC ACCCCAGTGA GTCTCCTATC ACTGTATCCT AACATTATTT TCTCCATGGC 1980 CCTCATCATT ACCTGCTGAT ATACTGTATG TTTGTCTATA TGTCATCTAA CACCCCTCAC 2040 ACTGGAACAC AATGCCCGTG GGCAGAGACT TTGCTAGCCT TGGTTCCAGA GCCTAGAACA 2100 GTGCCTGGCA AGTAGGAGAC ACCCAGCATT ACCTTTCTAA GTGAACCAGT AGAGATGGGG 2160 GGAGACCGCA AGGCTATGCC GGCAGACCTG AGGGAGTCCT GTCTGCATGC GCTGCAGGAT 2220 GACCTGAGGG GAACTCCTTG GACTTCTGTG CCCTCTTTAT CTGTAAGGTG GCCACCTGAT 2280 CCCTTCCAGC GTAGGCATGA AGTAGCCTAA TGAAGAGCAT TCAGGCTTGG GTATCAGTCT 2340 CAGGATCCTG GGGGCCTTAG AATTTGTGGC GCTTGGGGAC ACCTTGTGAT CGTGCAATTT 2400 CTGTTGTCTA 2410
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