Tag | Content |
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EnhancerAtlas ID | HS121-33702 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr7:50685840-50686860 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY2 | MA0748.1 | chr7:50685958-50685969 | AAATGGCGGTC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAAAATGGGA AAAAACAAAT ACGTAAAAGG TTAGCTTCAA AGTGAGGGAA GGTATGTCAT 60 ATAGATATGT CAATTTTAAA ACTATTCCTA CCAGTATAAT TACATACACC TGTATTTAAA 120 ATGGCGGTCC TTTTTATTCT CCTATCACAC AGAAGAAACA CCTCCTTCAA AAGGTTGTAT 180 TTTGTTTCCT GAAATGCTGG GTACTAGTGT GGAATACCAA CTATGTTTAC TAAGGGATTC 240 ATGTCTCACA GCATGCTCCA TGGCAAAGAG CGATGCCAGC GTCCCAGCCC AGTGGCACAA 300 GTGCACAGCG TGAGATAAAG AATTCCTGAA ACTAAAAGGT AAGCCCAGTC ACGAGAAAAG 360 CCTGTTCTGC TGCATTCCCC AAAAACAGTC TTCAAATTTC TTACTTTGGA ATAAAAAAGC 420 AGCTACATTA TCAGAGTCAG AAATGGCCCT GGGTCTTCTC CCCAGTTGAT GCAGCTCTGA 480 CCCATGACTC AGGATGACAG CGAGTGCCCC AGGAGCTAGG AGGTGCCCTC CCTATCCTGG 540 CCTCTCACAG GACAAGTGCC TCTCCCAAAG AAAGAAAAGA GAGATCAAGG TGACCAGCTC 600 AAGACACCAA CCAATCGCAC TGATTTCTCT AGTCATTCTT CCACGTATGA TCACAAAATA 660 TATTTGCTAT TTGCAGAGAA TAATGAGTTT TTCTTCTGCT AAGTGTTTGA TCAGTTCAAC 720 TGAGAACTTT CAAAATAACA GAAAACACCC AGCCTCTCCC AGCTCCTGTC TTAGAGACTA 780 ACCCCCTTTA CACTGTGTCT ATGTGAAGAA GGAGACCTCT ACCTTCAGCC AGTCCCACGC 840 ACATTTAGTG AAGCATGAGA CTGGGTTTCA AGCAAGGACT GCTTCATTAA ACTACAACTC 900 TGATTCTCAA ACCCATATGC TACACCATGC CTCTCAGTCA CTTTCTAATC TGATACTATG 960 AAACCCAAGT ATAAACTTCA AGATTTCAAG AGTCCCAAAC CCCAAACCTG AAGAGGTAAG 1020
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