Tag | Content |
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EnhancerAtlas ID | HS147-30851 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr4:44532200-44534050 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr4:44533993-44534008 | AATATAAAAATAGCA | + | 6.49 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGTCTGTTT CTTCACTTAT GAATTCAAGT GCCTAGAACA GTGTCTGTCA CCTAAAAGTA 60 CCACATAAAT ACTTGTGGTA CTTAGTTTAG GATGCTATAC CAAAAATACT ATATACTGGA 120 TGGCTTAAAC AGCAAATAAT TATTTCTCAC AATTTTGAAG GCTGTGAAGT TCAAGATCAA 180 GGTGCTGGCA GATTTAGTTT CTGGTAATGA AACTTTTTCT GGTTTGCAGA GGTACACCTT 240 CTTGCTTTGT CCTCACATGG TATGGAGATC ATATCTCTTG TGTCTCTTCT TGTAAGGACA 300 CTGATCTTGG CTTGAGGGCT CCACTCTCAT GATCTAATTA CTTCCCAAAG GTGCCACCTC 360 CAAATATCAT CATATTGGGG ATTAGGGTTT CAACATATTA ATTTTGTGAT GACACAGACA 420 TTCTGGTAGT CCCTACAATA ATATATTTTT AAAACTTTTA TTTTAGTTTC GGGAGTACAT 480 GTACAGGTTT GTTCTATAGA TAAATTGTGT GTTGTGGGGG TTTGGTGTAC ATATTATTTT 540 GTCATCCAAG TAATAAGCAT AGTACCCAAC AGGTAGTTTT TTGATCCTCC CCCTCCTCTC 600 ACTTCCGCCC TCAAGTAGGC CCTGGTGTCT GTTATTCCCT TCTTTGTGTC CATGTGTACT 660 CAATGTTTAG CTCCCAGTTA GAGTGAGAAC ATGCAGTGTT TGGTTTTCTA TTACTGCGTT 720 AGTTTGCTTA GGAATATTAT AGCCTCCAGC TCCATGCATG TTGCTGCAAA GCACATGATC 780 TCATTCTTTT TTATTCCCTT TGTATATATA CCACATTTTC TTTATCCAGT CTACTATTGA 840 TGGGCATTTA GGTTGATTCC ATGTCTTTGC TATTGTGAAT AGTGGTGCAA TGAACATCCG 900 TGTGAATGTG TCTTTATGGT AGAACAATTT ATATTTCTTT GGGTAAATAC CTAATAATGG 960 GATTGTGACC TTACAATGAT GCCTGCACAT TTAAGGAGAC AGCCAGCTCT TCTGACCTTT 1020 GCAGTGTTCT TCTGGTGGAG ACAGACCTTT AGTATTTAGT GTAGTTGAAT GGTACTTCTG 1080 TATTAAGTTA TTTGAGAAAT TGCCAAACTG CTTTCCACAG TGGCTGAATC AATTTACATT 1140 CCCAGAAGTG TATAAGCATT CCCTTTTCTC TGCAGCCTCA CCAGCATCTG TTGTTTTTTG 1200 ACTTTTTAAT AATAGGCATT ATGACTTATG TGAGATGGTA TCTCATTGTG GTTTTGACTT 1260 GAATTTCTCT AATGATTAGT GATGATGATC ATTTGTTCAT AGGCTTGTTG GCTGCATGTA 1320 TGCCTTCTTT TGAGATGTGT CTGTTCATAT CCTTTGCCCA CTTTTAATTT TGCTTTTGCC 1380 TCCTATAACT GTGTTCTTAA TCTACCTATA ATCTAAAAAT TTCAGTAGGT CAAGTTAAAA 1440 TTTTCTTCCT CAGCTAAGGT AATTATTCTT CAAAGAGTAC AGGGAGGGCA GATATATCCC 1500 ATGGAGGAAC ATTCTCAGTC CCTCTTCAGC CTCTCCAGAT ACAGTCGTAC ATTGCTTAAC 1560 AACAGAGATA CATTCTGAGA AATGCATCAT TAGGCAATTT TGTCATTGTG TGAACATACA 1620 CAAACTTAGA TGGTATAGCC TACTACATAC CTAGGCTATA TGGCACACCC TCTTGCTCCT 1680 AGACTACAAA CATGTATAAT ATGTTACTAT GCTGGATATT GTAGCCAGTG TAACATAATG 1740 GTAAGTATTT GTGTGCCTGA ATACAGAAAA GGTACAGTAA AAATATGGTA TAAAATATAA 1800 AAATAGCACA ACTCTATAGG GCACTTACCA AGAATGGAGC CTACTGGATT 1850
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