Tag | Content |
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EnhancerAtlas ID | HS037-07369 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr11:110434900-110436600 |
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) |
HEY2 | MA0649.1 | chr11:110436589-110436599 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr11:110436589-110436599 | GACACGTGCC | - | 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 |
GH11I110564 | chr11 | 110435352 | 110436928 |
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Enhancer Sequence | CAGAACATTT CATGTTCAAA AGCATTTTTC TTGGGGAACA GGTGGGAAGG AAAGACTGCA 60 AAACTTGAAT CCATTTTTTG TCACTTGTTT GTATTTCCAG AAAAAACAAC CTTGAGGTGT 120 TTTAGTCCTA TGGTGCGTGT GCTGGGCGCT GAGCTGTGCA GTGGGAGCCT CACATGAGAA 180 TCTGAGAGGT TCACAATGGA TGGGGACACA GAATGAGCCC CCGAGCAGGC TGCCACGGGT 240 GTCTAGCCTT GTGACCTCTC ATGGCTGCTT TTGTGATTTT TGTTCCCCCT CTACATCCCC 300 AATTTTTAAC ATACCTTTCA CCAAAAAACT CATGTGATTG TAGGTAGTTT ATTTTGTCAG 360 GAGTCAGACC TTACTTTCCC ACATGTTAAC ATGGATTCAT GAATTACATA CAACCAAAAG 420 TAACTGCCAT TAACCTGTGC AGTTTTATAA TTGGCTTTTT AAAAATGTCG AAAATGTTAT 480 GGGTATCCTG CTCCTACCTC TGAGAAACCC GAGCAGTCTG AGACCTTGGA AGGACGGTCC 540 CTGCTCACTG CAGTCCACGT CTTTGAGAAG AGCTACAAGA GGGCAATCTT TTTCTTTTTC 600 CTTGCTTTAA AGTACAGTCC CTCTTAAGAG CAGAGGGGGC AGGCAGGGAG TCTCTTTATG 660 ATGCAGATTG CCGATTTGTG ATGGGAATGA TCTAAAGTTT TTGATAGGTG GAAAACATCC 720 GCTCCCATGG TACCCAGCTG AGTTTAGGCC TAGAAGTGTT AAGCTGGACC ATACAGGCTG 780 CCCCTCCTCC AGCCAGACAT GGGGGTTCAG CCTGATAGCC CAGGGCTCCT TGTTATTGCC 840 CTACAGAGGA GTGTTCAAAA CATAAAAGTG GTCTGAGAAA GGCAGCAATC TTGTTTTCTC 900 ATGTCTCCTT AGTTTATGGA GAAGCCAAAA AACTCCATAA CAAATATTCA AATCCAGACC 960 CTGTCTCCAC CCTGAGATGG GTCCCCAGAG CCTGAGTGAG ATGCGATATA ATCTGGAGAG 1020 GGAGGAGATG AGGGCAGGAT GAAGTGGCGT GGGAGGCGGG GTGGAAAGTG TAAGGTCCTT 1080 GCCTGGCTGT GGTATCAGCA GTGAGTCCAG CAAGCAAAGG GTGTTAAGGG AATGAACTTG 1140 ATCCTTGAGG CCTCAAAGCA GGAGTGGTCT CTGTTCTCTG TGTATATCTG AGAGAGGAGT 1200 TGGGAGGTGA GGAGGCAGCA AAGATAAGAG GCCAGTGGCT GGGTGTCGTA TTACAAAGCT 1260 GAGAGGAAGA AGCGAAGAAA CGAAGAGCTC TCTCAAGAAA GATCAGAGAA AGCTGTGATT 1320 ATGCAATATG CCCACTGCAG ACAGACAGGC GGCACTGGCC CTTCATCTTT CTTAACCTCA 1380 GATTCCGAGA GAGCCTTTGT AGCCTGGTCA GTCACACACA GGCATGGGCT GGGCTGGGCT 1440 GGGGTGAACG TCAAAGCCCT GGCAGGTCTC ACTCTGGATA AGAGGGTAAA CCTGGGGAAA 1500 ACCGAAGACA TTTCCAGGTT AGGGAACTGA TGCTCAGCCA CAAGCCTGGT TATCAGTTTC 1560 CCACATTTAG CCCCCTTCAA GTTGCCCCCA CCCTCCCAAC CAAGTACCCC AGGCCTCTAA 1620 AGCTCCAGCA CTGCAGATGG TAGCGTGTGC AGTGCCCCAA CCTGCCACAC ACTTGGCAGG 1680 CCCCACCCAG ACACGTGCCA 1700
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