Tag | Content |
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EnhancerAtlas ID | HS105-53557 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:41404930-41405900 |
Target genes | Number: 14 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr22:41405697-41405708 | GGGCGGGAAGA | + | 6.14 | ESR2 | MA0258.2 | chr22:41405669-41405684 | GGGCCAAGCTGACCT | - | 6.52 |
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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 |
GH22I041008 | chr22 | 41404931 | 41406002 |
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Enhancer Sequence | TCATTTAGTA AATATTTCCC AAGCCTCCTC CATCCCTCCG CCACCCAAAA TGCCAGGCCC 60 TGTCCTGCAC ACTGGGGACC CATACATCCA TGGGTCACGG ACCTTGCCCC AGAGGAGCTC 120 TGGTCCCACG GCCTGGGCAA TAAGTGTCCC TGTGGGCTTC ATTTTTGTTT TCTATTTTTT 180 AAGAGACAGG GTCTTGCTCT GTTACCCAGG CTGGAGTATA GTGGTACCAT CACAGCTCAC 240 TGCAGCCTCA AACTCCTGGG CTCAAGTGTT TCTCTTGCCT CAGCCTCCCA AGTAGCTGAG 300 ACTATAGGCA TGCACCTCCA CGCCTGGCTA AAGTTTTGTT TTGTTGGTTT TTTTTTTTTT 360 TTTTTTTTTG AGCCTCTATG CCCCAGGCTC AAGCAATCCT GCCTATGTTG CTCAGGCTGA 420 CCTCACACTC CTGGGCTCAA GCCATCTTCC ACCTCAGCCT CCCAAAGTGC TAGGGTTACA 480 TGCATGAGCC ATCACATCTG GCTCCCACGG GGGGTTTTGT AAACTGAACA AAGGGAGCTC 540 CCTTTCCCCA GCAATTCATC CCTGGAGTCC ATATGAACCA ATGTTCCTCA TTTACAGCAG 600 AAAAAGCAGC TTCCCATGCT CTAACCCCTG CCTGCTCCTC AGCTGAATGA GGCTGACAGG 660 TGCACACCCT GCAGCATCCT GCACCTCACC AGGTAAACAG GCCTGAAAGA GGGAGGCCAT 720 GGGTGTGGGC ACAGGCTCAG GGCCAAGCTG ACCTCGCAAA GGCTGAGGGG CGGGAAGAAC 780 AGGAGGAAGT GTGGGCAATG GGGAGCTGCT GGGTCTGGAG CAATTACCAT TGCCACATGG 840 TGAAGACACC AGCCCAGAGG CTGACCTGGG GCTGAGCAGA GCCCAGCAGT AGGGTAGGAA 900 GGGGCCCACC CTTGCTCCTC CAGCTCCCTT TTCTCCCCAC CCCTCAACCC CAAACTCTGT 960 CCCTCCTCCT 970
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