Tag | Content |
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EnhancerAtlas ID | HS059-29871 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr21:43662310-43663460 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr21:43662405-43662420 | GAGTCCAAGGCCAGC | + | 7.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTAAAAAG ACTATACAAT GGGCCTGGCA CAGTGGCTCA GGCCTATAAC CCCAGTGCTT 60 TGGGAGGCCA AGGCAGGAGG ACTGCTTGTG CCCAGGAGTC CAAGGCCAGC CTCAGCAACA 120 TAGCGAGACG CTGTCTCTAC AGAAAATAAG ATGAGCAGAG CATAGTAGTG TGCACCTGTA 180 GTCCCAGCTA CTGAGGAGGC TGAGCGGGGA GGGTTGCTTG AGGCTAGGAG TTCAAGGCTG 240 CAGTAAGCTA TGATAGCACT GCTGCATACT CCAGCCTGGG TGACAGCAGA GACCCTGTCC 300 CTAAAAACAA AACAACACAA AAACTCAAAC TGCACAATGA GAGAGGAGGA GGGAGCTGTA 360 TTATAGATGT GTGGTACCTG GAACCAAGTG GTGACGCTGA GGAGGGCGGA AGGAGCATGA 420 TGAGAGGTGG CTGGGTGACT TGGCTGCTGG AGAACGCTGG CCATTAGGGC ACATTCATTC 480 TGTTCCGGCT CTTGTGTTAT TTCACACTTT CCACATCCCA GTCCTTTAGA GCCGACCATG 540 AACCGGGGCA GTGAACCATA TCGTTGTTTG TTGTGTTTTT TGGTTTTTGT GACTTCAGAG 600 GCTGAAGTGC AATGAGGCAA TCAAGCGAGC TCCACCATGG CCCTGAGGGC TTGTGAAAAT 660 GCAGGTGGCT GGGCTGCACC CCCGGGGGTC TGAGTGAGCA GGTTTGGGGC AGGCAGGGTT 720 CCGTGTCTGA TAAGTATGGG GCGATGCTGC TGTTGCTGGT CCAGGGATCC CACTTTGAGA 780 ACTGCTGAAT TAGAGTAAAG AGGAGTTGAT GGCCATGTGG GAGCCACCCT GAGCCCTGGG 840 AAAACTGGAG CAGGAGGTGG CATCACCCAC ACTTGCACCA CAGGCAGGAG TGAGGGCCCT 900 GCTCTCCCAT GGTCAGGCAG CCTCAGCATC TCACCACTCC CTGGCCTTCA AAGTCAGCTT 960 TCCTTGTGAA CCTGGGTGGT CAGAGATGCA GACAGCAGGG CCAGGTGGTG TCTCACGAGT 1020 CGCACTATGA ATGTGGGGAG CCCGTCGGCC CCTCCCTCTG CAGGGAGGAG AGTTAAAGCT 1080 CATGTCCTCC AGGGTACCTT CCTCGGGGGT GGTGGACTGC TGCACGCCAG GGAACAGGGC 1140 AGAAGTGCCT 1150
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