Tag | Content |
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EnhancerAtlas ID | HS034-20802 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr3:46941070-46942000 |
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 |
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Enhancer Sequence | AGGCCTGCCG CCCTTCTGTG ATCCTGACCC TATTCCAGGC TCAGGAAACA GCAGGGCTTG 60 GCCAGGGATC AGGTTCACCT GAGGTTAGAT TCACCTGAAT TGAGGCTCGG CCCAGGAGAG 120 GGAAAGGAGG AACCATCAGG CCAAGATTCA GCTCAGGATC AGAGTAGGAT ACTGGGTCAG 180 AGGTCAGCCT GGGGCTGGAA TTGGGATCCG GGACCCTCCC TCTACCCTGA GCCCCATGGA 240 CTAGGCCAGC ATCTATTACC CCACCAGTCC CCTTGCTGGG ATGGGGCGCG GGGCTGCCCA 300 CACCATTGCC AGCCTCAGCA GGCCTGCGGG GTCCATGGCC CAGAGCCGTG GGCCCAGCAC 360 CTCAGCATCA CCTGAGCTTC ACAGCACCTC TGCAGAATGG GTTGCTGGAG CTGCGCACTC 420 CTCCCAGCCC CCCACAGGCT CTGGGATCCA GTTACCGATA ATTGTCCATT ATTGTTGGCA 480 GCTGCAGAGC TTGGCTGGGC TCCGGGACAA CTGGCCAGAC TGCAGAGGGG TGGGCCGGGT 540 GGCTGGAGCC CTCTCTGCAC TCAGCACCCA GAGGCCCACA GGTCAACAGC CACCGCCTCC 600 CTGCCCCTCG ACATACATCC TGACCCTGAC CTCACCATGA CAAGCCCCAG AGTTGGGGAG 660 ACCTGGGCCC AGTCCCAGGA ACAGATGCAG GCTCTGGGGC TAGGAGGTGT CCTAGTGGAC 720 TGGCGACATG CAGATTGGGA GTGCATAGAA TCCTGGGGCA CAGGAATGTC ACAGCTCTTT 780 TTCTTACCGT AAAGCCAGGT CATACCCTAT CCCTCCAAGG GTGTACCAGG CCTAGAGTCA 840 AGTTGGTGGT ATGTGGTCGG GGAGGACCTG GGGCTCCCTT CCCAGAGGCA CAGCTCACCC 900 AAATATACCA TGTGCCCCTT GAGCTGGCGC 930
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