Tag | Content |
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EnhancerAtlas ID | HS098-38490 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:46940950-46941940 |
Target genes | |
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) |
NR2C2 | MA0504.1 | chr3:46941241-46941256 | CTGGGTCAGAGGTCA | + | 6.85 | Nr2f6 | MA0677.1 | chr3:46941242-46941256 | TGGGTCAGAGGTCA | + | 6.37 | Rxra | MA0512.2 | chr3:46941242-46941256 | TGGGTCAGAGGTCA | + | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I046898 | chr3 | 46940035 | 46941004 |
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Enhancer Sequence | GCGGGCACAG CGGGTAGCGA GGTGCCGGCA GGGGTGGGAC CGTGGGTGAC AGGGAGAGGG 60 CAGCCCCTGG GGGGAGGCGC CCACACAGCA CATCCCGCCC CAAGTGGAAC AGCAGGAGAG 120 AGGCCTGCCG CCCTTCTGTG ATCCTGACCC TATTCCAGGC TCAGGAAACA GCAGGGCTTG 180 GCCAGGGATC AGGTTCACCT GAGGTTAGAT TCACCTGAAT TGAGGCTCGG CCCAGGAGAG 240 GGAAAGGAGG AACCATCAGG CCAAGATTCA GCTCAGGATC AGAGTAGGAT ACTGGGTCAG 300 AGGTCAGCCT GGGGCTGGAA TTGGGATCCG GGACCCTCCC TCTACCCTGA GCCCCATGGA 360 CTAGGCCAGC ATCTATTACC CCACCAGTCC CCTTGCTGGG ATGGGGCGCG GGGCTGCCCA 420 CACCATTGCC AGCCTCAGCA GGCCTGCGGG GTCCATGGCC CAGAGCCGTG GGCCCAGCAC 480 CTCAGCATCA CCTGAGCTTC ACAGCACCTC TGCAGAATGG GTTGCTGGAG CTGCGCACTC 540 CTCCCAGCCC CCCACAGGCT CTGGGATCCA GTTACCGATA ATTGTCCATT ATTGTTGGCA 600 GCTGCAGAGC TTGGCTGGGC TCCGGGACAA CTGGCCAGAC TGCAGAGGGG TGGGCCGGGT 660 GGCTGGAGCC CTCTCTGCAC TCAGCACCCA GAGGCCCACA GGTCAACAGC CACCGCCTCC 720 CTGCCCCTCG ACATACATCC TGACCCTGAC CTCACCATGA CAAGCCCCAG AGTTGGGGAG 780 ACCTGGGCCC AGTCCCAGGA ACAGATGCAG GCTCTGGGGC TAGGAGGTGT CCTAGTGGAC 840 TGGCGACATG CAGATTGGGA GTGCATAGAA TCCTGGGGCA CAGGAATGTC ACAGCTCTTT 900 TTCTTACCGT AAAGCCAGGT CATACCCTAT CCCTCCAAGG GTGTACCAGG CCTAGAGTCA 960 AGTTGGTGGT ATGTGGTCGG GGAGGACCTG 990
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