Tag | Content |
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EnhancerAtlas ID | HS052-02010 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:95267040-95268380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:95267481-95267502 | CTTTAGTTTCACTTTGTATCT | + | 6.3 | NKX2-3 | MA0672.1 | chr1:95267687-95267697 | ACCACTTGAA | + | 6.02 |
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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 |
GH01I094801 | chr1 | 95266548 | 95270865 |
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Enhancer Sequence | ATTATTATTT ATGTAGTCCT TCTGTCTATA ACATGTAGTT AATTCTTGCA CAGTGTATGT 60 AATATGCAGT ATCTTTAGGC CACTGAGTGT ACTCCACAGA AGTCATCCTT CTGTCACTGT 120 AACCCTATCA CGTGCACTGA TAACACAAGT ACTCCCAAAA TGACCCAGTC TCCTTTTGAA 180 TTTGATAAAT TGCCTGAATA TACACTTAGG TAAATTTTAA CAATACTTTG CCAAGCCTTC 240 TACCCCACGA AATAATCCTA GTGGATTTAG TTTGAAATAG CATTAAATGT ACAAATTAAC 300 TTTGAAACAA GTCCTATCTT CACAATGTTT TCCTTTCTTG ACATGATGGG CCTTCTGTTT 360 ATTCCAGCCT TCTTTCGCAT TGCTCATTGA AATTTGTGCC TTTATTTCTA TCTGTTACAT 420 TTGTTTCCCA TTCTGCCCCC ACTTTAGTTT CACTTTGTAT CTTCCCATTT CCTTAGAGAA 480 TGAACAGCCA CACATAATGC AATAGGACTT TTATTTAGGG TAGATGAGAA ATCCTAGATC 540 AGTTTTCATT TTACTAAACA ATTAGTTAAC AGAAGCATTG CCTAAGAGGC CTGTGCTCTA 600 ACTAGAACGG CAGAGTTCTC CAAGTCATTT GTTTCATCTG GTTAATAACC ACTTGAAAGC 660 CCTGTGCTCT CTTTCAAGTT ACTTGGCTCC ATCTTCTGGT TTGAATTATG AGTACTTGGA 720 GTAAGGGCAG TTAAAAGTTG CCAGAGCAGG GCTGAGACTG GGGTGAGGTG AGTTGCGCAT 780 CTAGGGTCCA GATTTAAGGA AGCGTCTGCT CTCAGGCCCC CTGGTGCCTC GTCCACCACA 840 CCTGGTCCCA GCCTGCCCCA GGGAACCGGC TGCTGTGAGC CAGCTACCAT CTGGCAAGCA 900 GTTGGGAGAG GGAGCCACCG TTTCCCCCAT AGCTCTGCCC TGGGCCTGCA CAGTGGGAGT 960 TGCTGTCACC GTCCACAAGG AGCACTTGGC CCAGCCTGGC TAATGGGCCC CACTCTTGTT 1020 TCTCCAGGTC ACTTTTGTGT TTTGTAGATG CAAGAGCCAT CTACAGCTGG AACCGACTGA 1080 CAGCCCAACA CCATCTAAAT GCTCTTACAA GATCCGTAAA GCCAAATCAT TTCCATTTGA 1140 GAAGCACTTT GTCTGAACTG TGTTATTGGT CCATGGGTCA TGACCTCCCT CTAGCCTGTG 1200 CCACCCTAAC TGCCCTTAAC TGTCCAGAAC AACAACCACC CCTGCCCCTG AAGCCTTCCC 1260 TGAAAGGCTT CAAGCACAAG AGCTCGTTTT TTAAAAATCC AAGAAGAGCT GAATATGAGC 1320 AGATGAAAGC AGCTATAATA 1340
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