Tag | Content |
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EnhancerAtlas ID | HS067-00157 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr1:32107760-32108850 |
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) |
Stat6 | MA0520.1 | chr1:32108735-32108750 | GTGTTCCTCAGAAAT | + | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 32108514 | 32108709 | chr1 | 32108000 | 32108400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I031642 | chr1 | 32108020 | 32108204 |
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Enhancer Sequence | GAGACGGAGG TTGCAGTGAG CCAAGATTGT GCCATTGCAC TCCAGCCTGG GCGACAGAGC 60 AAGACTCTGT CTTAAAAATA AACAAATAAA TAAAAAATTT TTTTCAAAAA AGGGAAAACT 120 GAGTCTCAGA CTTTTGCAAC AAACTTCTGC AAGGGAGTGA CAAAGCAGGG ATTTGAAATC 180 AACTCTCTCT GGCCTCAAAA ACTAAGCTCT TAAGCACTGA AATCCACCAA GCTCGTTCCC 240 CCATAGGACC AAAGGGTGCT TGAATTTTAC TACTCCAATA CCCAGTCCCT GCTTGGGTAC 300 CCTGGACTGG AAGCAGTGGA AAATTACAGG AATTCTGACT CCTAACAATA GGCTGGAATC 360 CTCCAAAGCT ATGTAGTGGG TGGAGGGGAG GCAGCACTGA CTGAGATGCT TTAAAACAAC 420 TCGTTTCCTT TCTTAGAACA CCTGAGACCA GGAGGCGGAC AAGGGTATGG TAGGAAAAAA 480 AAACAACATT TCTTTTTCTA TTCCAGACTC TTCTCTCTGT GCTCCTTTTC AGTATTTCAC 540 TCCAGGAATA GCCCAGGCAG CATGGCATCA TGAGAGCAGT CACGGCAGCA AGAGCTGCCA 600 CCAGACACTG GCATGTACTA GGCACTAGCA ACACGCCAGG CTCCCTGCAT TTTAACCTCA 660 TTTTAGCCCT TTTCACAGGT ATTATTTCTC CCTTTATACA GGTGAGGAAG CTGAGGCTCA 720 GAGCCCTTAG TTTGTCCAGG GGTATATAAC TATTAAGTAA TACAGCTAGA ATTCTAGCAC 780 AGTTCTCTCT AACCTGTCAC TGCTTTTAGG ATGCACACCA ATTGTCCCTA ATGCTTATTA 840 GCATGTAGAT TCCTGGGTAC AGAACAGGTC TGAAGTGGGA CCCAAAAGTG TGCTTTCTTA 900 AACAAGCTCT CAGCTGATTC TGAGGCAGAA GACCAGCCAC TGGGAAACAA GGCGCTATGA 960 ATGTTTTTTC AGCCTGTGTT CCTCAGAAAT ACTAGAGTCA AAAAAGTGAC CAGACATCTG 1020 AAAAGAAAGC CGGGAGGCGG AGTTTCTATG GTTAGATATG TTTAAGAAAT ACTGCATATT 1080 ATATTCCTTT 1090
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