Tag | Content |
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EnhancerAtlas ID | HS041-14617 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr3:49917990-49919040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr3:49918726-49918741 | GAGGGTCAAGGGTCA | + | 6.42 | Nr2f6 | MA0677.1 | chr3:49918727-49918741 | AGGGTCAAGGGTCA | + | 6.77 | RFX1 | MA0509.2 | chr3:49918503-49918519 | TGTTGCCATGGCAACC | + | 8.25 | RFX1 | MA0509.2 | chr3:49918503-49918519 | TGTTGCCATGGCAACC | - | 8.29 | RFX2 | MA0600.2 | chr3:49918503-49918519 | TGTTGCCATGGCAACC | + | 8.48 | RFX2 | MA0600.2 | chr3:49918503-49918519 | TGTTGCCATGGCAACC | - | 8.51 | RFX5 | MA0510.2 | chr3:49918503-49918519 | TGTTGCCATGGCAACC | - | 8.48 | RFX5 | MA0510.2 | chr3:49918503-49918519 | TGTTGCCATGGCAACC | + | 8.59 | Rxra | MA0512.2 | chr3:49918727-49918741 | AGGGTCAAGGGTCA | + | 6.87 |
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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 |
GH03I049880 | chr3 | 49917861 | 49920130 |
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Enhancer Sequence | GCTAGTGTGT AGTGGAGCCA GAATCTGAAG CCAGGCCACC AGGCTCTGGA TTCATACTTC 60 AGGATCCTGT GTTGCCACCA CTGGGTGCCA TGCTCAGGGC CAGGCAGTCA CAGACCCTGC 120 TGGAGGGGAG CTAAAATGAC TCCATTGTGG GTTCTGCAGC AGCAAGCCCT ACACCCAAGC 180 TGGGTCCTGC ATGGACCTGC TCCTCCTCCT GATAGCTTAT CAGGTAGCTC AAGCCTGAGA 240 GGAGGCCCTT CCAGGAACCT GGTGGTGCTG AGTATGGGCC AGACTGAATC CTTCGTATTC 300 AGAATTCTTA GCTGGCCAAA GCCTGCTCAT CTCATCCAGC TGGGGAGAGG AGCAGCAGGG 360 CAAATAAAGA GGCTTTCAGG CTGGGTCCCT TCTTCCCAGC CCCTAGGGAT AGCGCCCCTC 420 GGCCCCTCCC CCAACATGTT TTTAAATAGT GTCTCACCAG GAAGAAGGGC GTCCAATTCT 480 ATTTCTGAAT CTGGGAAGTG AGGAGGGCCA ACGTGTTGCC ATGGCAACCT GGAGAGCCCC 540 TCCCCCAGAC TGAGCCCATT CCCCAGGCTG AGGGCTGTGG GGTGGGAGGG AGGTGGCAAG 600 GAGGAGCTGG GAGGAGCTTA GTCTGTGGAT GAGGCCAGAT GGCGTCCCTG TGAGGGCAAG 660 TCCTGCATGA CCTTCTCCTC ACACTTCACC TCACCCCTCT AGGCAGGCTT GCTAGGAAGG 720 CCCCAACCTC TGCAGAGAGG GTCAAGGGTC AAATCACTGT GAGAAACCCT TCTCCCCTGT 780 GGATCAGGCT GGAACCCTCC CACTTAGGAG GTCTTGAGGA TAGTAGAGAG GTGGCAAGAA 840 GGGCGTCAAG GGGAGAGGCA CAGCGCCACA CCCTATTAGG AGCTCTACAG CTGGCTCCCA 900 CACCTGCTTC AATACAGACC TATTTTCGGC TCCCTTGTGT TCTCAGGAGG CAGCTAGCTT 960 TGTCAAGCCC CTGGCCTTGC ACCCGTCCGG TCTGCCTGCC TTCTACTGCA TTGGGAAGGG 1020 TCTGGACATC TCCAAAAGCT AGGATCAGAA 1050
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