Tag | Content |
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EnhancerAtlas ID | HS089-08963 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr3:39413810-39415340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chr3:39414385-39414397 | CAAGATGGCAGC | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGTGCCCCT CCCCCAGCCT CGCTGCCACC TTGCAGTTTG ATCTTGGACT GCTGTGCCAG 60 CAATGAGCGA GACTCCGTGG GTGTAGGACC CTCTGAGCCA GGTGTGGGAT ATTATCTCCT 120 GGTGTGCCGT TTTTTAAGCC CATTGGAAAA GCGCAGTATT AGGGTGGGAG TGACCCAATT 180 TTCCAGGTGC CGTCTGTCAC CGCTTTCTTT GACTAGGAAA GGGAATTCCC TGACCCCTTG 240 TGCTTCCCGG GTGAGGCGAT GGCTTGCCCT GCTTCAGCTG GCACACGGTG CGCTGCACCC 300 ACTGTCGTGC ACCTACTGTC TGGCACTCCC CAGTGAGATG AACCCAGTAC CTCAGTTGGA 360 AATGCAGAAA TCACCCGTCT TCTGCATCAC TCACGCTGGA GCTGTAGACC AGAGCTGTTC 420 CTATTCGGCC ATCTTGGCTC CTCCAGATTT TCTCACTTAT TCTTGAAAGA ATTTTTCCAG 480 ATTATTATTG TTAACCCAGG AGGCTGTCAA ATTAGAAATG AATCTGTGCC TCAAAAGTTA 540 AAGAAACCAG TAACTAATAG AAATAATTGA GTTTGCAAGA TGGCAGCTAA GAAAGAAATA 600 ATTTGTTGTT AACACTGAAA CTCTCTCTGC TTATGAGATA AAGTAACTAA CATCAGTTGG 660 AATCAATATG GCCAGTGCAT GTCTGTGCAG AACCAGCTTG CTGACATCAC CACCTGAATT 720 TATATGAAAT GATTCATACT AACTCCCCTT GAATTTGCAC ATGTGATCCA TGAGGTATCA 780 TGAAGAGACA ACTGCACATC CCCAGAGACT TTCCAGACCT CCACTTTTCT TCCACCAATC 840 ACCTAATCTC AAAATCCACC CCCTGAAACT TTTCTAATAA AGATACTGCT TTGAAGCCAG 900 CACAGAGAGA CAGATTTGAG CTTCACACTC CTGTCACCTT GTGAGTTAAC TTCCAATAAG 960 ACGTCTTTCT TCTCTCAAAA CCTGGTATCA TAGTATCGGC TTCTAGTGCA TTGGGCAGCA 1020 AGCTCCCTTT AGCTTGATAA CAGAGTCTCA GAGTAGAATG TCTTTAAAAT CGTCTCTACC 1080 CTGCCTCCTG CATCAGCCAG CTAGTCCATG CTTACACATG CCCTGTGCTT TCTCAGCTTT 1140 GCTGTCCCAC TGCCTGGCCT ACAGCAGGCC ATGCCCTGGA AGACTCAATT CTGAGTGCAG 1200 CCAGCCCTAT GAGAGGAGCC ACCACACTGG GCACAGCAGT ATTGGATCAG CTCTGTGATT 1260 GGGGTGAGAT TTGAAGAGAG GTCTCCTCCA CCTTCTGCCA GACTGCTGCC TGTCAGGACT 1320 ATTCTCTCTC CGACCCTAGC AAAGACTATT TGGAAGAGCC AACACTTGTG AAGTGGAACA 1380 TATTGCTGGA TCTTGAATCA TTCCAAGCTT TCCTTAGGGG ACACTGCAAG GGATATATTG 1440 GAAGACCTGT CCTGGACCCT GCTCCTTCAC TTACAAGCCA GCCTGAACTA ACCTCTTTGA 1500 GGTTAGTCAC TGGTAAGATA GGGATGATGA 1530
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