Tag | Content |
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EnhancerAtlas ID | HS034-18489 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr20:24851480-24852750 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr20:24852249-24852264 | TGCCCTCTGACCCCA | - | 6.95 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCTGTTCTC TGCAGCCCTC ACTCCTGGAG CCCTGGCCAT GTCAGAAGTC CCGCTGTGAT 60 GAGCTGCCAC ACGCAGAGCC CCTGAGAGGG CGCTGGGGGA TGACACGGCC CCCCGCTGCC 120 AGACTTGGGC TTTCCCAGCT GAGGCCCCAA CACTGTGGAG CAAAGTCCAG CTGGCCCCTG 180 TATCCTCCCC AGCCCAGACT CACAGAAACT ATGAGCACAA CAAAATGGCC ACCCTGGGCC 240 CCCTGCTGTA GGGTCAGCCT TCACACAGTG ACAGTACTGC AGCTGCGGTG GCGATTGCCC 300 TGAACAGGGC TGGTCCAAGG GCAGTGCAGT CACCCCTTGT GGTCCTTGCA CAGCTGTGCT 360 GAAGTCATGC ACCGCTGACC ATGCAGGGAC AGGCTGAGCA TGGGTCATCA CAGCCCCACA 420 GATTCTCCCT CACCAGGAGG CACGATCTCA TGTTTCTGTT ATGTTTGGGG GACTTGTTCA 480 GGGATCTTAA TTATAAATAA GCACTTTATC GTGTTTTAGA TACATTTTGG GGACTTGCAT 540 GGAGGGTTTA GGGCAACAAG CAATGCATTA TCATTTTTCC CATTTAAAGT AATGGGAGCA 600 GGCTCCCGGT TTGTGCTGTC AGACAGGAAG TCTCATTTTA GCAGCAGATT GTCAGCATCA 660 AGCAAGCCAT GCTTGGACTG GCCTCTGCCC AACCTGTGTG GGTGACGCCC TCAGGACCCC 720 ACATGGAGGC GCACTGTTGG CATCAGGCTG TACTCAGCCC AGGATCTTAT GCCCTCTGAC 780 CCCATCAGAC AACATCAAAA ATCCCCTCGA GGTACCACCC TTCTGCTGGA GGGAGCCCCT 840 GCTCCTGCCC CAGGCACAGG GTGCTTTGAG AATCTGCCGG CTAAGCCTGC ACATCCTGCA 900 GCCACGGGCA TGCCCCAGGC CAGTTCCTCC TGCTTCCACC TTCCTCCCTG CCCCTCCTGG 960 AGCCCGGGCT CCCCAGCTGC CCCTCAAGAC CCAAGTATCC ATGAGGAGAC GCCAGAGGGA 1020 AGGGAGTGTG GCTGGATGTG CAGCGAGGGT GGGAAGACCA GAGGGTGTCA GTGGCTCCTA 1080 ACTCCCACTC ATTGCCTTTC CTTGCCAAGT CCTCCTTCCA GAGCCTCCTG CTGTGCGCAG 1140 AAGGAGAAGA AGGGAGGGAC AGGAGAGGAG CTGGGAGGTG GGATGGGGGA GGCACAGCGA 1200 GGCTCTGAGA TATTTCTCAG GGGAGCAAGT GCAGCCCTAA GCAAGGCGGG CCATTCTGGG 1260 CTGGGGTTTT 1270
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