Tag | Content |
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EnhancerAtlas ID | HS105-55317 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr3:46687720-46688790 |
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) |
FOSL2 | MA0478.1 | chr3:46688383-46688394 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr3:46688383-46688394 | GGGTGACTCAG | + | 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 |
GH03I046646 | chr3 | 46687869 | 46688941 |
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Enhancer Sequence | TGTGGATTAT TCCACATCTA TGTAAATTAT AGATGACCAC ATGCTAGTAA GTGATAGAAG 60 GGGGATCTGA AGTCAGGTCT GTGAATCTCA GCCCTGCTCT TTCTGCTGCG AAACAGAGTA 120 CCTGGAAGAA ACGCTGTACA GCATGAACAA AATGTCTGCA AGTCTAAATG ATTCCAATGG 180 GCCAGTCTGT CCTGTTGAGT TGAAGGTGTT TCAACGGGTT TTATTATTCT TTAGGTGTGA 240 TGAGGCCGAG ATGAGGAGAT GACTGCTATT GGAAACATAG CTTATCATGC CAACAGGTCC 300 CAAGAGAGGG AGCCCCCATG ATGCCATGGT GGGGTCACAT GGGGAGGCAC CAGGGTCAGT 360 CACAAGAGGG GCTGGGGAAC TGTGGGCAAG AGTCTGAGTT GTGTTTTCTG CAGGAAGGAA 420 TGGGCGAGGC AGGGTGAGTA GGTAATCTCC GCAGGCTCTG GGGCACAGGT GCTGTCCTTG 480 GTTGTCTGGT ACCTGGCCCT GAGGTGATTA GGGCAGGAGG ACAGTGGCCT GGATCATGAG 540 AGCCCAGTTA GTACGGTGTG TGGACTCTGG ATTGGTTGGT TTGTATTTGA AAAGCACATT 600 CCTGGGAGGA TGACTTCTCT CGAAGGAGGG AGAGGAGGCA GTGAGCAGGG AAGGGCCAAG 660 GCTGGGTGAC TCAGGCATGT CACAGGGTTG TCCAGAACAA GGTGGATCTG GCATACACAT 720 GCAGAGCAGA TGTTAAGCTT CCATTTATAG AAACTAGAGA CGTGATTGAT CCAGAAGGGC 780 TATTTCTGAG GCTCTATCCT TCGCTATACT GCACAGGCAT CCCCTTAAAT GCCAGTTCTG 840 CGGGTATCAG AAAAGAGGAC ATCCTCGCTC CAGGAGATTC CTGTGTACAA GTAGGCCTGG 900 GATTTCCATT TCCAGCCTCT GAAGCTGACA GGCTCTGTGA GTGACGGGCA CCCGTTCCAG 960 GGTCCTAGTG GTCTCAGCAC ACACAGGGCT CCACTTCAAA GGTGATTTGG TAAGTGCTCA 1020 AGTCCTGAAT GTCCTCCATG ACCTCGGAGA GAAAGAAATA GGTTTGGATA 1070
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