Tag | Content |
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EnhancerAtlas ID | HS108-00349 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:11756850-11758600 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:11758110-11758130 | CCACCACCCACCCACACACA | + | 7.89 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 11757451 | 11757508 | chr1 | 11757890 | 11758200 |
| Enhancer Sequence | CCTGGTTTCA GTGAGCCAAG ATCGCGCCAC TGCACTCCAG CCTGGTGACA GAGCAAGACT 60 CTGTCTCAAA AAACAAAAAC AAAACAAATC AAAATAGCCA GGCATGGTGG TGCATGCCTG 120 TAATCCCAGC TGCTTGGGAG GCTAAGGCAG AAGAATCACT TGAGCCCGTG AGGCAGAAGT 180 TGCAGTGAGC CGAGATCGTG CCATTGCACT CCAGCCTGGG CAACAGAACG AGATTCCATC 240 TTAATAATTA AAAAAAAAAA AAAAAACAAC TTTTACTCCC CAATCCTCAT GACAGCTAAC 300 ATTTTACAAG AGAGGAAACT GGGGCCCAGA GAGGTTAAAA AACTTGCCCA GGTTGTCTAG 360 CTCCTTCTGC TTTGCTCAGT GAGGGCCCTC CCATGGGTCA GCTTAGTGGG TTTGGGCTGA 420 CATCTGTGAG CTGGAATCGG TAGTAGTGAT GTCTGGGCCT CCACCTCTCA TTAATGAGAC 480 CTGTGGCCTC TCACCCGGAC TGTCTCCCTT ATCAGTGGGG ACACCTGGAG GCAAGGACTG 540 TGTCTTTGCT GGCAGATCAG CAGCTCCATG TTCTGGGACC CTCCCAAGGC CAGAGTTGTG 600 CCTCTCCTAT CAGATTGGCA AATTCCTGAG GACAGCAACT GTATCTACCC TGCTAGATGG 660 GAGGCTTCCC CAGGGCAGGG GCTGCTTCTG GCTTAGATTG AAAGCACTCT GCAGCCATGG 720 GCTAGGTCCC CTAATAGTCA TAGAGTCCTC TAAGGCATGA CCTGGTTCCC TCCTATCCCA 780 ATGAGCCAGG ACTATGTGTC CGCCCTCAGA CTGGTGGTTT CCAGGAGCAG AAGCCAGGTC 840 TCTCCCTTCA GACTGGAGCA GGTGCCCTTG TCTGGCATCC TGGTTCTGCA CACAGAGGGG 900 CTCAGCTAGT GGCTGACCAC CGGGATTCAC TCTCCCCTGC GATCTCCATC GCAAGGAGGC 960 AGCAGTCCCC AGCAGAGCAA AAGGCAGAGC TCTGTGCCTG AGAAAGACCC GTGGAGGGGT 1020 AGGTGGGGCT CTGGCTGCTC TGAGGCCTAG GGGTTGCTGA GAGGCCCCTT CCTATTGGTC 1080 AGGTGACACT TTGGGCGATA CAGAGCCACA GGGAGGCAGG GAGATGGGTA GGGACTAGTC 1140 CAGGATGATC AACGCACCAG TATGCCAGTG AACACCCAGC AGGGCAGCTG CTGTGAATCC 1200 CACCCGCCCC ATCCTCTATG CCACCTGCAC TGCCGGGCTC CATCCATACC CGGAACACCA 1260 CCACCACCCA CCCACACACA AACCACACAG AAGCACTGAC TTCCTAAGTA GTCAAGTCTC 1320 ATGGCAGCCT AATAATCCCA TTTCACAGAC AAGGGAATAG ACTCATGAAG GGAGGAGATG 1380 TTGGGAGGGA TCAGGAGGGG GGTTAGAACA CTCTCGTTTC AAATTACCTT GGGAAGAGCT 1440 CAGCCCAGGA ATTAATTTAG AATCCATACA GTTGTTCCCC AACTCTCATG TAGGATATGA 1500 CTGTTTTGAC TGAACAAGAA AATTACCCAC TTTCCAGCCC TAGGGGTGTC AGCTCCACCT 1560 AAACAAGACA GAAGTCTGCT CCTAGGGGGC CGGGGCTCCA GGAAGCCCTA ACTAGATCTG 1620 GGGCTGACTG CAGAGTGGCC ACACTCTGCT AAGAGCAGAT GGGGCTTCCG GACTGCACTG 1680 CCCATCTCCA ATTCCTGCCG TTTCAGGAAG TGTCCATGTG AGTGATGAGG AGTAGCCAGA 1740 GGGAAAAGTT 1750
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