Tag | Content |
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EnhancerAtlas ID | HS102-13163 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr2:121257200-121258440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr2:121257213-121257228 | TTCTATTTTTGTCTT | - | 6.49 | SP2 | MA0516.2 | chr2:121257444-121257461 | GCAAGACCCGCCCACTG | + | 6.12 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAGGTTTAA CTTTTCTATT TTTGTCTTCC CATGGTTTTG TTTGCTGTTT CCCTCCCTGC 60 CATCTCTCTT TGGGAGGGAG TGTAATCCGC ATAGAGAGGA GAGTCTTTTA TATGACTTGA 120 GATTCACAGT AGTTCACAAC TCCCACCTTT GTCACCGTCA CCCTGGCATC TTGAACCTAA 180 AGTCACTTTC TGCTCTCCAT GGCATCTTGA ACCTAAAGTC ACTTTTATCT TTTGGCCCCG 240 CCTTGCAAGA CCCGCCCACT GCTGTGGCCC ACTCAGGAAT CCCGGACACC AAGTCTATCC 300 CCCGGCATCC CCCTGCACTC CATGCCTTTG AGCATGGAGC ATACATTGAG TGCTGGCTTC 360 AAGTTCCCCC ACCCAGTCTG AGCCAGAGCC CTGGAGAGAG GGTGGCAGGG ACCGATGGAC 420 CCTTCTCCAG ATGCACACAG CCCAACGTCA GTGCCTCTGG TTGTGACTGT CCCCTACTGT 480 ACAGGCATTG GTAGCATCTT TGCCACGTGT ACACAGGCTT AGGGCAAAAG TCCCGTGGGC 540 TGATTGGTAA GCTGAAATAG TGCCTTTCAG CCTTACACGT GCTCTGTAAT TGCAAGGAAA 600 GCAGCCCGGA GGCCGGCTCC TACCCTCTGG TGCCTCTGCG GTCCCATCTC ATCTCAGGTC 660 CCTCCTCTGC TTGTCCCTCC TGGCCCCATG CCCAGTGACC TATTTCCACC TCATTCCCTT 720 CTCTCATCAC CTGTGCCCTT CAGCACTTTG CAGTTGAATA TGACTCAGTT CCGGCCTTTA 780 AGGGGCCCAC AGTGCAGTGG GTTCTCAGGC AGCCTGTGGC CACTGTGCCA TGCTGATGTC 840 TTTCCCCTGT GGGCTGGACA GTGGGGACTT TCTGGCTACT GGGCCCATCG TCACATGCAC 900 ATGCCTTCTT GCTTTTCTCC CTGGAGGCTG GGACAATGTC TTGCCATGGT TCTGTCCCTC 960 ATCCCTGGTC CTCAGCCACG GCCATTGCCA GTCAGTGCTT TGTGTATTAG CTGCTTAGTA 1020 AATATGCCCA AGGGATGGAT TGTAGGCTGT GGAGCAACAG ACAAGGGAAG CCCCAGGTTC 1080 TGGAGAAGCC TGTGCCCAAA GAGGGGAAGG TATTTGCCCA AGATCACAAA GCTACGGTGG 1140 ATTTTGTATG TATTGATTGT AGTGCTTTCC AAATGCTCCA TTTACTCTGG GATTAAATGA 1200 GATATTCCTT GAAAAGCAAA TGCTTGACCA TAGTAAGCTC 1240
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