Tag | Content |
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EnhancerAtlas ID | HS052-00779 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:29564420-29566860 |
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 | chr1:29566333-29566351 | TCCTCCTTCCCTCTTTCC | - | 6.4 | Gfi1b | MA0483.1 | chr1:29565563-29565574 | GGCTGTGATTT | - | 6.02 | Six3 | MA0631.1 | chr1:29565709-29565726 | AGATGTGATACCCCTTG | - | 6.35 | ZNF263 | MA0528.1 | chr1:29566333-29566354 | TCCTCCTTCCCTCTTTCCCTC | - | 6.15 | ZNF263 | MA0528.1 | chr1:29565184-29565205 | CCTCCCACCCCATCCTCCCCA | - | 6.22 | ZNF263 | MA0528.1 | chr1:29566195-29566216 | CCTCCTTCCTCCCCCTCCCCC | - | 8.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 29565515 | 29565732 | chr1 | 29565762 | 29566055 |
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Enhancer Sequence | CGTCCGGGCG CGGGCAGGGC CTGGCTCGCC GCCGGGGGAC GGCGCCCCCT CCCTTGGCGC 60 GCAGGACGCG CGGGGGACGC CCGGGCCTCC CGGGACACTC CCTTGGTGGA GCCTGCAACT 120 TTGTGCGGCC TCCCGGCCGG CCGGGACCGC CAGGTGTGTG CTTGAGTGTG AGCGTGAGTG 180 TGAGCGTGTG GCTCCGCGCT TGTCTGCTGT GTGGTCGCGT TCTCCGGGTG TGTTTCGGAG 240 TCTGGTGTCT TTGGTGTGCG TGCGCGTGTG TGTGTGCGCG CAGCTGAATG TATGTATACG 300 GAGCCTGTGT TTGTGTGTCC GTGTGCTCGT CGGAGTGTGG ACGGTGTGTC GGATGTGTGT 360 GCGTGCGCGT GTTCCACATC CCACCCTGAG GCCTGGGATC CTAGACCGCG GCCCCTTCCC 420 GCGGAGTTTC GGGGCCCTGC TCCGGGTGAC CTCCCCCGCC CTCGCCACCG GCGGGGCTGC 480 TCCGCGGGCT CCGGGTAGCC GGGAGACGCC CGGGGCGGGA TCCGAGCCGA GACACGTGCT 540 GGAGCGGAGC CGCTTCCTCA CGGTCGCCAG CCGCAGACAA CTGACCTCCC CGGCATCGCG 600 TTCGCGGCCC TGCTGCTGGC TCCGGTGTCT CGGGCCGGAA CTCCTGTGGC TCCAGCGTTC 660 GCGCCGGCCA CTGGCCAGCG CTTGGGCCTC GCCCTGCAGC TCCGGGGCCA TAGGGCACAG 720 CTTTAGCTTT GACCTCCCCG TTCCCGAAAG GACGCCCAAG GCGACCTCCC ACCCCATCCT 780 CCCCAACTTC TCCCCCATGT CCTGCGGCAA CTTTGCCTCC CTCTCCCACC GTGAAATCAA 840 ACCCGCGGGG TTCTGTATGC GCCCCATCCC CGCTCCTACC ACCATCGCTT TGATTTCAAG 900 AACACTCACA AGCCCCAAGC CCTGCCAGCA GGAGGACTGT CAGGAACTGA AGTTTGGGAG 960 TGAGGCCTAG AGCAGGTTAC TCCCATTCTT GATGCCTCAG TTTCCTCTTC TGCCTCATAG 1020 CCATCATGAT AATGGTGTAT GGCACTTTTG GTAGATACCA AGTACCTTGT AAAGTAAGGC 1080 TCTGTCTGTG AGTGCCAGGG AACAAAAAAT GGATTTGAGA GTTGTTGCAA AGCCCCAGAC 1140 AGAGGCTGTG ATTTAAAGCT GGGGTATTAG GTGTCAAATT CTGCCTCTGC TACTTGCTAT 1200 TCATGTGATG TCTGGCAAAT CACCTCACTT GTAAAGTTCC TGGCCCCCTT TGTTATTCTT 1260 AGAGATGAAC TCAGAAGCCC AAGTAGAATA GATGTGATAC CCCTTGTCCC CAGTCTGGAC 1320 AGAGTCAGCC CAGCTCCCTG AATGGCTCCG GAGCTTCCGG GTAGGGGCGG TGTGTGATGC 1380 CTTCTCAGCC TTGCAAACCT GGTAGTTATT TATTCTGCTG TGTTCTTGCT ATTTTGTCCT 1440 TTTGGTCGCA GGAGTTGTGG ACGGCAGGAA TGAGGGAGTG GCTGCCCAGT GGTTTCAGGT 1500 TGGGCAATAA AGGCTTGTCT GGGCATCCCT CCCTTTTCCC TGGGGCTAGG GGAGGGGACT 1560 TAGCAGGAAG CAGTGACAGT GGCCGAGGTG GGGACGCTGA GCTCCTGGAC AGCCTGCTGC 1620 CCAGCTCTGG TGTCAGAAAA AACCTAGGGC AAGCATCGTG CTTGATGGAG ACAGGCCACC 1680 ATCCTTCCAT GATTTTCATC AGCTCAGCTG GGCATATGGG GTGGCCTTTC CATGCAGGAC 1740 TGGGTTGGCC AGAGTTGCAG GGGGTACCTT GTGCTCCTCC TTCCTCCCCC TCCCCCCTTT 1800 TCCTAGTTGC CCTCCTGCAT CCTGGAACGT CCTGTCTGCC CTCTCAGAGA CTCTTTCATC 1860 TGTCTCCTTC TGTCCGTCCT CAGCTATCTT TCACCTGCAG GAAGACTCCA GCCTCCTCCT 1920 TCCCTCTTTC CCTCATGGTG CCAGGGATCT TTGTAAAGTA CATTTTAACT CAAAGGGTTT 1980 AAAACCCTTT GAAGGCTCCC CATTGCCTTC AGGGTGAAGT CCTTATCCCT TGGCCCTGTT 2040 GCTGGCTCTA GCTCCTGCCT GCCTGTCCAG CTGCATCTTG TTTTGTGTCA CTGCCCCTTG 2100 CATCCTATGA TCTGGCCAGC CTGACCTTCT TACCAAAGAC CCAAATGCCC ACAGCCTGCT 2160 GTCTCCTCTC TGGGCCTTTG GGCAAGCCGT GCTTTCTCTG CAGAACTTTC TAACTCCAGC 2220 TTTTTGCTGG TGAACTCCTG CAACTTGATG GGCTCTCAGC TGTAAGCATC ATCCAGTCCC 2280 TGAAGCCTTC CTCGGTGATG CCCTGTCCTA GCCTAGGAAG TCGGGGGGTG GGGGTCAATT 2340 GGATTTTTAC ATAGCATTGT AATTATTGTA ATTACAGTTT ATTAGTGCTG TCTCCCTTAC 2400 CAGACTGAGA GCTGAGGACA GAGACTGGGT TTTTAGTTTA 2440
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