| Tag | Content |
|---|
EnhancerAtlas ID | HS105-47705 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr2:219274000-219274940 | 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 | chr2:219274778-219274793 | AATATAAAAATAGAC | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTAACCAAGA TAGTCTCGAT CTCCTGACCT CGTGATCCAC CTGCCTCAGC CTCCCAAAGT 60
GCTGGGATTA CAGGCATGCG CCACTGGCCC ATTGTATCAT TTTTTAAAAT TTGTTTTATT 120
TAAAAAAAAA TAGGTCCAGG TGCGGTGGCA CATGCCTGTA ATCCCACCAC TTTGGGAGGC 180
CGAGGCAGGT GGAACACCTG AAGTCAGGAG TTCAAGACCA GCCTGACTAA TATGGTGAAA 240
CCCTGTCTCT ACTAAATACA AAAAAAAAAA ATTAGCTGAG TGTGGTGGCG CATTCCTGTA 300
ATCCCAGCTA CTTCAGGAGG CTGAGGCAGG AGAATCGCTT GAAACCGGGT GGCAGAGGTT 360
GCAGTGAGCG AAGATCCTGC CATTGCACTC CAGCCTAGGC AAAACAAGAG CGAAACACTG 420
TCTCAAAAAT AAATAAAATA TAATAAAATA GAGACTGGGT CTCACTATGT TGCCCAGGCT 480
GGTCTCGAAC TTCTGGGCTC AAGTGATCCA CCCACCTCAG CCTCCTAAAG TGCAATGATT 540
ACAGTCTTGA GCCACTGCAC TCAGCCCATT GTATCATTTG TAATAGCAAA ACACTTAAAA 600
TAATCTAAGT GTCCACCAAT AAAGAACTGG TTAAATACAT TTTGTTATTG AATACCATGT 660
AGTCGTGAAA ACTATGAGGA GGAACTATAC AAGCTGATAT AGAATGATCT CCAAGAGATA 720
CTGTTAAATG AAACAAGGCA AGATTCATAA CAATGATGGT GTACTCCTAT TAAGGCAAAA 780
TATAAAAATA GACGCAAATA TAAATATATA CTTTCACTTA CTCTGAGAAG ATAATTGTGG 840
CTAATCTTGG GGAGTGAGGC TGGGGGAGTG AGATTCATCT AATGTATAAG AGACACATGT 900
TATTACATAT CTGTTTGTAA TTTGAATTAT TTTACCAGGT 940
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