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EnhancerAtlas ID | HS105-65156 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr5:112551100-112551800 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr5:112551312-112551329 | GAGGACACAGTGTTCTT | - | 6.05 | Ar | MA0007.3 | chr5:112551312-112551329 | GAGGACACAGTGTTCTT | + | 6.31 | NR3C1 | MA0113.3 | chr5:112551312-112551329 | GAGGACACAGTGTTCTT | - | 6.38 | NR3C1 | MA0113.3 | chr5:112551312-112551329 | GAGGACACAGTGTTCTT | + | 6.42 | NR3C2 | MA0727.1 | chr5:112551312-112551329 | GAGGACACAGTGTTCTT | - | 6.27 | NR3C2 | MA0727.1 | chr5:112551312-112551329 | GAGGACACAGTGTTCTT | + | 6.55 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATGGTTTGA ATACTGCACC CTTCAAAATT GAGGTATTGA AACTCAGTGG CCAATGTGAT 60 AGTGGTTAAG GGTGGGGGTT GGTCTTTGGG AAGTGATTAG GTTATGAGGG CTTTTGCCCT 120 CATGAATGGG ATTAAGGCTC TTATAAAAGA CGGTTCATGG GCTGGCGGGG GAGGGCGGTT 180 CGGCTGACTT GCCCTTCTGC CTGCCATCAA GTGAGGACAC AGTGTTCTTC CCCTCCAATG 240 GATGCAGCAT CCAAGCCCTC TTAGAAGCAG AGATCAGAAC CTCAGCAGAC AATAAGCCTG 300 CCGGCGCAAT GATCTTGGAC GTTCCCAGCT TCCAGAAATA ATAAATAACT TTCTGTTCTT 360 TATTAGTTGA CTAGTTTCTG GTATCCCATT ACCTCTCCCT TCACTACGAG AGAGCCTCAG 420 TTACTATCTC CAGGCCAAGT TGAAGCCATT AGTTAGTCAT TCTACAAATA TTTAGTAAAT 480 GCCTACACTC AGTAGGGGCT GGAATGACCA CACTCTGATC TCTCAAAGAA ACCACCAATC 540 GCTTTGTTGT TCAATCAAAA CTGTTGTTTC TCAGTTATAT CTTGTTTGAT GGCAAGCCCT 600 TCTCCTTTCC CTGTTCCAGA GGTCAGGAAA CTATGGCCCA TGAGCAAAAT CTGACCTTCT 660 ACCTGTTTTT GTGAATAAAG TTTTATTGGA ACATAGGTAT 700
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