Tag | Content |
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EnhancerAtlas ID | HS150-00490 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:62802210-62804660 |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:62803502-62803520 | GAAAGGGAGGGAGGGAGG | + | 6.13 | NFYA | MA0060.3 | chr1:62803790-62803801 | TCTGATTGGCC | - | 6.02 | NFYB | MA0502.1 | chr1:62803791-62803806 | CTGATTGGCCCGGCT | - | 6.16 | SOX10 | MA0442.2 | chr1:62803136-62803147 | AAAACAAAGAC | + | 6.14 | ZNF263 | MA0528.1 | chr1:62803504-62803525 | AAGGGAGGGAGGGAGGGAGAG | + | 6.58 |
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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 |
GH01I062336 | chr1 | 62802093 | 62804728 |
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Enhancer Sequence | CCTCCACTCC TCCAATAGGC CCCAGTGTGT GTCATTCCCT TCTACGTGTC TGTGTGTTCT 60 CATGATTTAG TTCCTGCTTA GAAGTAAGAA CATGCGATCT TTGGTTTTCT GTTCTGCAGG 120 GTCTCTCTTA AGATATTCAG AACAGAGGAA AAAGCAGGAG TTAGATGGGT CTTGAGTGAC 180 TCTTTCTAGG CCAGCGTCCT TGTTTCCCAA GTCCAGTTCT CTTCCCCCAG GCTCCTCCCC 240 TGGGAGCCTG GAGGCCCCTA CACCTGGAGG AGCCGGGCCA AGGTTGGATG GCTGCCTGCC 300 TGCCGAGGGC ACTGTAGAGC GGGTGGTGGG TAGTGGATGA GGGTGGCACT TGACGCTGAG 360 ACCCCGCCGA CAGCCTGGGC ATCCTTGACT CGGGAAGTTA CACAGAGTGA TGGACCTTCC 420 TGTTAGGACT GTTTTACTAT AAATGAAACA GGAAAATATG AGAGAGTTCT TGAACTCTCC 480 TGGGAGGAAG ACAGTAACAA GCCATCTGAC CACCCAACTG CAGCTCACTT TAAATAACTT 540 TCTATGGCTA TTTTAAGACA GAAATGGACA TTCTCCTATT AATAAGCCTG GCTAAGTAAG 600 GCTGATCTGC AGCCAGGGTG AATCTGAAAG CCTCCTTCCC CACAGAGTCC CCAAGGGCAA 660 CAGACAGAGG GGCGTGCTCT TGTCGATGGA CAGGCCCACA CTGGTCATTT CGGGCAGGAA 720 ATTCTGTAGG GGAAGAGATT CCTCAACCTC TTATGCCTGC TCTTGCCCTT CTTGGAGGAG 780 CTCAAAAGCA GAATTTCTGT GGCTGAAAGG AGGATTTCCC CAGGGCCAGG CGTTGCCTCT 840 CCCAGGCTCC GCACTGACAC TCCTGGACAC TCCCACAGCC TAAGGAAGGA GGGTCTATTC 900 TTATTCCCTC CTTCCTTATA GATGTGAAAA CAAAGACAGG GGAGAGTTCA TTCTTCTCCA 960 AGTTCTCACA GTTAGAAAGG GAAGCTGGGA ATTGAGAGGG TTGCAAGTCA CCACTCCCCA 1020 CCGTGCCTGC CCTCCTGAGG CACGGTTTAG ATGCTGCCCA GGCCTTCGAA GCCAACTTCT 1080 TGCTTTGCCT GGGCAGTGGT GGGAGGCGGC TGCTCATCAC CGCTGGGCTC TCCCTTTCTT 1140 GCTCACTTGG CTCTTTGGTG TCCTTGTCAT AACTGAAAAA GCCATCATGG GCTGACGACC 1200 AGGTCCCCTT CACCCCAGAA CCATTTTGTG GGAGTGGTCA CTGCCCGGCT CCCCTCCCCT 1260 CCTGTGTCAT CAGACACTCA GTCACCCAAA GAGAAAGGGA GGGAGGGAGG GAGAGCCTGG 1320 GGCAGGGGCA GAGGCGCCTC AGCCTGACAT CATGGCTTCT GTCTGTGTCA CTGCCTTTCT 1380 CCTGCCTTTC CCAGTCTGAC TTCTCACTGT AAGGCTTCTA CTAGCCAGTT CTCTGCTTCC 1440 CCCATCTCTC TCTTCCTCAT AGGCCCCCCA GCTCTAGCTC CACCATCTGG AATCTTCCGA 1500 GGAGTTCCTG TGGCCTCCAG TCCCGCAGCG GACAGACTGC ATGTCTCAGC ATTTCTTGGT 1560 TCAAATTCCT GAGGCAGGAA TCTGATTGGC CCGGCTCCCT TTTCGTGCTG GGCCACAGGT 1620 CATAGGTTGC TGGCCAGCCT CAGTTGGCTG TCCACGGACA GCCAGAGTTG AGTGGGACAA 1680 AACACAGCTG AGGAATGTCC CCTCCTTTCA GCCGAGGCTG TTTGTTGAAT TGTTCCTTTT 1740 AGAAGGGACA ATGGCCAACA TTTGTACTGT GCTTCTAAAG CCTCTGCTGG CCTGAGGCAG 1800 GAACACAGTC TTTTGGGTCC TTTATAAATA ACTGTTTTAA CTGCTAGAAC AACTTACAAT 1860 ACGAAGGCTC TCACTCCAGC TTTCACTACG GCGTACCCCA TCTCTTTCAG ACTCCTCTCC 1920 TTGCCCCAAA TCTGTCCCTG GGAGCCCCCA GTGGTGACTC AGGGGTGAGT CCAGTCTGCA 1980 GCCGACTGCC TCCCACCGCA AATACTGCTG GCCCCACGAC CTTTGACACT TGGATTTTAG 2040 CAGCGGTCAC TCTATCTCCC GGCCCCAGAG TCGCCTCTGC CGACGGCCTC AGCATACCCA 2100 AGCCCTGCCA TGATTCAAGG AATAGCCACA GGGAGAGCTC TTCTCCCTGT TTGTGGGCCT 2160 CACCCCCTAT TAAATAGGAT TTTAATACTC GGGCCCCGAT GGCTTAGGGG CCGGAATGCC 2220 TAGTTTTTGC TCGAAGGCCA CTACGCCCAG GATCCAGCAC AAATGCCTGT GAGGCCAGGA 2280 CTGGGGATGC AGGGGCAAAG TTAAGGGGGG GACAGCAGGA CTTCCCTTGC CTGGGCCTGG 2340 GGGTGACCGC ACTTGACTTG ATTCCCCTGG GAGAAGTTAT TTCCCCACAG ACTCCTTGGT 2400 CTCTTGGGCC GTAGACTTGG GTGGGCCTCC CCAGAAAGTC TGGCTCTCAG 2450
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