Tag | Content |
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EnhancerAtlas ID | HS053-00267 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:10078270-10079280 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr1:10078823-10078840 | CAGGTCACAAAGACCTT | + | 6.09 | ESR2 | MA0258.2 | chr1:10078824-10078839 | AGGTCACAAAGACCT | + | 6.63 | IRF1 | MA0050.2 | chr1:10079230-10079251 | ATGTACTTTCATTTTCAATAA | + | 6.49 | Lhx3 | MA0135.1 | chr1:10078620-10078633 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr1:10078624-10078637 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr1:10078621-10078634 | AATTAATTAATTA | - | 6.78 | Nkx2-5(var.2) | MA0503.1 | chr1:10079193-10079204 | CTTGAGTGGCT | - | 6.62 | POU6F1 | MA0628.1 | chr1:10078622-10078632 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:10078626-10078636 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:10078622-10078632 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr1:10078626-10078636 | ATTAATTAAT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 10078632 | 10078732 | chr1 | 10078826 | 10078938 | chr1 | 10079057 | 10079172 |
| Enhancer Sequence | GACACAGCGA GACTCCGTCT CAAAAAAAAA AATAATAAAT AAGAAAAGGA AAAAAAAGAA 60 TACAACTCAG GAACAGCCAA ATGGAGGAGA TGCATGGGAC AAGGTTTAGT GGGGGGCTGC 120 GGAGCTTCCT TGCCCTCTGC AGGTGCACCA CCCTTGCAGT GCGTGGATAT GTTTGAGGCA 180 GGAGACCAGG GTCTGGAGGC AGGGAACCTA AGGCTGTTTT GGGCTGACTT CCTAGAACTA 240 AATTGAAAAG AAAATCCTAA CTTTCCAAGC CTAAGTAACA AAAGGACCAG AGGCTACCCC 300 TTTGCAAACC CCTACCTTTT CTGTGGCAGA TGGGAAATTG TAAGTACCTC TAATTAATTA 360 ATTAATTGCC TTTTTTTTTT TTTGAGACAG AGTCTCTCTC TGTTGCCCAG GCTGGAGTGC 420 AGTGGCACCA TCTCGGCTTG CTGCAACCTC CACCTCCTGC GTTCAGGTGA TTCCCCCACA 480 CTTACTGGGC TGCATTCCCA GAAGGTTAAG GCATTCTTAG TCACAGGATG AGATAGGAGG 540 ACAGCACAAG ACACAGGTCA CAAAGACCTT GCTAATAAAA CAGGTTGTGG TAAAGAAGCC 600 AGGAAAACCC ACCAAAACCA AGATGGTGAT GAGAGTGGCC TCTGGTCTTC CTCACTGCTC 660 ATCATACACT AATTATAATG CATTAGCATT AGCACCCACC ACGCCCAGCT AATTTTTGTA 720 TTTTTAGTAG AGACGGGGTT TTACCATGTT GGCCAGGATG GTCTCCATCT CTTGACCTCA 780 TCATCCGCCC ACCTCTGCTT TCCGCAACCA ATCGGACTGA TTACAGGCCA CTACTTCACC 840 TCATTTACAT GGGTGAACAC CCAGTGGCCA ATGGGAAACC TCTAGTGGGT ATTTGGACTG 900 GAGAAAATTC TGTATCCAGG GCCCTTGAGT GGCTGCTGGG GCCCGCTCCC ACCTGGTGAA 960 ATGTACTTTC ATTTTCAATA ACTCTCTGCT TTTGTTGTTT CATTTTTTTC 1010
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