Tag | Content |
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EnhancerAtlas ID | HS094-40217 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr8:29360240-29362020 |
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) |
Ar | MA0007.3 | chr8:29361590-29361607 | TAGAACATGGTGTCCCC | - | 6.08 | NR3C1 | MA0113.3 | chr8:29361590-29361607 | TAGAACATGGTGTCCCC | + | 6.45 | NR3C1 | MA0113.3 | chr8:29361590-29361607 | TAGAACATGGTGTCCCC | - | 6.5 | NR3C2 | MA0727.1 | chr8:29361590-29361607 | TAGAACATGGTGTCCCC | - | 6.45 | NR3C2 | MA0727.1 | chr8:29361590-29361607 | TAGAACATGGTGTCCCC | + | 6.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 29361220 | 29361668 | chr8 | 29361105 | 29361688 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I029503 | chr8 | 29361220 | 29361668 |
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Enhancer Sequence | ACTGACCCTA TAAGTCCTCT TGAATGCTTG CTGAAGGGGA ACAGGAAATA TTAAATCTCC 60 AATTATGTCT TCCCCAGCTC CCCAAAGCAA CCTCAGAACA AGGGAAGGCA ATGCGGACAG 120 ACATCAATCC ATCCTCTCCT TCTTAACAGG ATGGAATCAG CTCGATTTTC ACTTGTGGGG 180 ATCATATGTT TTCCAAATAT GAGGGTCATT TTATTTTTCT TTGCCACATG AAACTCTATG 240 TGAAGACCAT GCCTTCTCTC TGTTCTCAGA GGGACCATTG TGGTGTTGGC ACCCAGTCAT 300 TTTTATGCAA TAATGGTGAA GGATTTAGAA ACGTGTGCCT TCTTGTCACT TATGTGCTTG 360 TTTATATAAA GTAAATTCCC TTTGTTTGAG AAGATTGAGT CTTCAGAAGA GGTAATTTGT 420 TTCCATCTAG TGGTTCACCC ACTGAAAGTC TTGAGCTTTG CACCAAGTTC TCCTGGCTCT 480 GGGTGACTTG TGTGTCCTGG TGTGACCACG AAGGCCACGG AGGGTGGTCA AATAACACAG 540 ACTGAGCACT CAGCAGCACT GCTACTTTGA TGTGATGTTT TTTCAAAATC AGCTCTGGAT 600 ACAAGCAAAT CATTTGTATA TTACCTGCTT CTGGGTCAGG GTTATTTTAA AATAGATCTA 660 GATGACCCCA TCCCAATCTG CAACCTCTTT ACATCACAGT GCTTTCAAAA AGGGTTCATG 720 GGATTCTTAC TTTTATATCC ATCTTTGGAG GTGTGTTAGG GCTGATGTTG GGGTTCAATT 780 TAACTCCCCA GGAGCGAGTA TATTCTTCCC ACTTTGCTGT GACACAGGCT TGTGTCTGGT 840 CTCAAAATCA GCTTCTCGTA GAGCATACTT CATCAGGCAG CAGTTAGTCT GTGAGTTTCA 900 ATTCGGGGAA CGACACTGGA GTCCATCCAT GAAATCTCAG TGACTCCCAA GAAGAAACAT 960 CACCACCTCT TGAGATCCTT CGAAAAGCCC AACCTTCCCA GACAGACTCC TTTAACCCAC 1020 CTGATGTCTG AGTCCAGTGT GCCAGGTATG TCACAGGGTA GCTGCCTGGA GGAACATGGG 1080 CCTCCTGATT TTTGAGAATG CTTGTGACTT GGCAGGGCAG CAGGACCTGA CTTGGCAAAG 1140 GCCATGTACT TCCTTTGTCT GTATTGAGGC CAAGTAAGAG AATTCAGGAA CATAAATTCT 1200 GAAAGATTAG ATTGAATCAG AACAAGGCAG CTGTTGTTTT GCCAGAGTTT AAAGGGCATT 1260 GCAAGGGCTG TTGGACCGAC TTCTGTTTTA TTTAGGGATT TCCCACCTCT CTCATGTGAA 1320 AACTATTGCT GTTGGCTTTT CCCTGTTGAC TAGAACATGG TGTCCCCCTT AGGAGGGAAG 1380 AGGTTGTGTC TAGACTTGGA AGGAGGACAG ACAGCCATCG TGCTGCTGAA GACTCAGCTG 1440 AGCAGTGGAG AGTGGCAGCC ACAGGGTGAT GGTCCCAGCT GTTCATCAAG ATGATCCCAA 1500 GCCTGGGAGC CTAGGTGACC TGTCCAACAT GAACCCCTGA CAACCTTCTC CCCCAGGTCT 1560 CAACTAGAGA GTTAGGACAT TTCTAGAAAA TGGTGGAGTA AAATTTTAGC ATCTCCCTTT 1620 CCTCCCCTTT TTAATATTCA TTGAATTAAG TTTAGGTTGA TTAATGGATA TACTCGCTTT 1680 TCCAGGAGCT TCCTTAGTAT TGACTTACAA TCCTGAATAT GACTAAAAAT CATGACGTTG 1740 CTGTTTCTCT CCATTTTCTA GTGTCCCCTT GTTTTGATCT 1780
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