Tag | Content |
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EnhancerAtlas ID | HS055-04013 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr2:1049860-1052110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr2:1051498-1051508 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:1051498-1051508 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:1051498-1051508 | ATTTTCCATT | + | 6.02 | ZNF263 | MA0528.1 | chr2:1051943-1051964 | TGGGGAGGGAGGGAGGGAGAG | + | 6.78 | ZNF263 | MA0528.1 | chr2:1051978-1051999 | TGGGGAGGGAGGGAGGGAGAG | + | 6.78 | ZNF263 | MA0528.1 | chr2:1052077-1052098 | TGGGGAGGGAGGGAGGGAGAG | + | 6.78 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 1050141 | 1050353 | chr2 | 1050705 | 1051873 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I001053 | chr2 | 1049462 | 1051935 |
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Enhancer Sequence | TTTCCCGTGG TGCGGCTCGG GGGTGTTCTG CCACCTTGTC AGGTGGTGGA AATTGGCCCT 60 TTCTCCTGCA TCCCTAAGCG TCAGACCTCA GCCGTTCCCA CCCAAGAGAG GCGGCCCACA 120 CCTGGGCTGT GGCTGGAGCA TCTTCACGGC ACCAGGAGTT CACTCTTCTT CGTGCCAAGG 180 AATTGGTTAA TTCTTCTAGG ATCTAGCATT TTTAATTATC TAACTCTAAT GAGGGGTTTA 240 CGTAGAGGGC TTCGGGGATT TTCAGTATGG CTCTCTATTT GACTGAGTTT GAAGGATTCC 300 TGAAAGGAAA TCCCAAGCTC CTACTGTGGT TTTGTCACTC TTCCTAGCAG GTTTAGGATG 360 CAGTCCTACA TGGCTAGAGA TGTTAGAGAA GGTCTCAGTA ATATCCCTGT GAACCCCACA 420 GAGCCGCCTT GGTGATTCTG GGACCCCCTG GAGGTGACAC ATTCCTGAGA CACCCCAGGG 480 TACACAGCAA TAGCATAATT AAGCCCCATG CTAATGAAGT CTTTTCCCCA GACCTTGGAT 540 CAGAATATCA CTTGTTAATA TTATCTGAAG TTAATGTTGA TGTATTTTTG GATTTTCAAA 600 GAGGTACATT TTCAAATGAA AAATCTAAAT TGGGAAAATG AAGAAAGTAA AACAGAATAA 660 TGTAATTGTA ATTAGGGTCT ACTATTAAGC ATTTGAAATA CATGAGATGA AAATTAGCCA 720 TTTTAGAAGT TAAAAATATT GCCAGGGTGA TGGCTTTTTT TGTTTTGTTT TTGTTTTTGT 780 TTTTTTTTCC CTATTGATTC CTTTGGTCTT TATTTCATTC AGAAAACAAT TGCCTCTCAC 840 CTCCTCTATC CAGCCTGCGT CAGGTACTGC TGTGTGAGTC TATAAATGCT GTTACCTCCT 900 CTGTGCAGCC CACGTCAGGT ACTGCTGTGT GTTGCTATAA ATGCTGTTAA CTCTGCATTC 960 ACATTGTAGA CGTGGCCCTG ACTGCAGGGA GCCAAGAGAG AAGTGGCTTC ATGTCATGGG 1020 CAGCGAAACA GGGGCTGTGT GAGAGGAGTG GGAATGTGAG CTTGCCCCGG CCCAGGCCAT 1080 CTGCCTGACT GTGCAGTTCA TGGCTTGGGG CCGCTCTGCT CGGGGCTTCT TTCTGTAAGT 1140 TTTTCATTTT GTGTAGGTGA CTTTTTCCAG TGCTGTTGCC TAGAGTGGGT ACCGTTTTCT 1200 GATGAGCCCA CACAGAAAGA ATGCATTTCC TCTCACTGGA GGCTCACGAC CTGCCTTGTG 1260 TCTGATGACC CACACAGAAA GAATGCATTT CCACCCACTG TGGAGGCTCA CAACCTGCCT 1320 TGTGTGGGTC AGGATTTTTC ATGGACGTCA CTAGATCAGT GTGCTGAATG CCCATCGAGA 1380 CAAAAATACT AATTTTGAGT CAGTGTGATG CCAGAAATGT TTTTATCAAG TAGCAGGTAC 1440 AACTATTTAT CAGTTTTAAT ATGAAAATGT TAGTCATTCA TAGAGATCAA ACCATGTTGC 1500 AGAAATTCAG ATTTGGAAGA AACCCGGAAC AGTAATTGAT CTTATCCATT CTCCTAGGGT 1560 TATCATGAAG GATTTAACAG TGTGAACATT TCCATTTTCT AAGGTGACCG TGCCTTTATT 1620 TTGATGGCTC TGAATTGTAT TTTCCATTCA GTTGCAGCAC CAGCCCTCCC TTGATGTGCA 1680 GAATGAGCAG GTGTCTTTAG GAGTGAGGCT GGGGCACGAC TGAATGCAAA TTAGCCCTTG 1740 CCCAGACAGA AGACAGTCTC ATCTCACCAG CGGTATTTCC TGGAGGGTCT GATCTGTCCT 1800 GGACATGCGG TGGGTCGCGG GGACTGCAGC TTCATCTCTC AGACGGCTCC TTGTCCCCAC 1860 TGTTTCAGAG TGGACACAGG GAGAAGGGGT GAGGCAGCTG GGACCCAGGC GGCTCCTCTG 1920 GCTCCCATCT TGGTGGGAAG CTGGTCCACA CCACCAAGAG CACGGGGAGG ACTCCCTGCG 1980 GATGGGCTCC AGCTTCATTC TGAAGGAAGG AGTTGAATAA GTTAAGGAAA GTGGATGAGA 2040 GGGAGAGTGC ATGGGGGAGG GAGGGAGAGG CCGCACTGTG CTGTGGGGAG GGAGGGAGGG 2100 AGAGGCCGCG CCGTGCTGTG GGGAGGGAGG GAGGGAGAGG CCGCGCCGTG CTGTGGGGAG 2160 GGAGGGAGAG GGCGGCGCCC CGCTGTGGGG AGGGAGGGAG AGGGCGGCGC CCCGCTGTGG 2220 GGAGGGAGGG AGGGAGAGCG CAGCGCCACG 2250
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