| Tag | Content |
|---|
EnhancerAtlas ID | HS098-33149 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr2:219273750-219275230 | 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 | TTTTTAATGC AGACAACTTT TTTTTTTTTT TTTGGATGGA GTCTCGCTCT GTCGCCCAGG 60
CTGGAGTGCA GTGGCATGAT CTCGGCTCAC TGCAAGCTCT GCCTCCCGGG TTCTCGCCAT 120
TCTCCTGCCT CAGCCTCCCG GGTTCTCGCC ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG 180
GGACTACAGG CACCCACCAT CACGCCCAGC TAATTTTTTG TATTTTTAGT AGAGATGGGG 240
TTTCACCATG TTAACCAAGA TAGTCTCGAT CTCCTGACCT CGTGATCCAC CTGCCTCAGC 300
CTCCCAAAGT GCTGGGATTA CAGGCATGCG CCACTGGCCC ATTGTATCAT TTTTTAAAAT 360
TTGTTTTATT TAAAAAAAAA TAGGTCCAGG TGCGGTGGCA CATGCCTGTA ATCCCACCAC 420
TTTGGGAGGC CGAGGCAGGT GGAACACCTG AAGTCAGGAG TTCAAGACCA GCCTGACTAA 480
TATGGTGAAA CCCTGTCTCT ACTAAATACA AAAAAAAAAA ATTAGCTGAG TGTGGTGGCG 540
CATTCCTGTA ATCCCAGCTA CTTCAGGAGG CTGAGGCAGG AGAATCGCTT GAAACCGGGT 600
GGCAGAGGTT GCAGTGAGCG AAGATCCTGC CATTGCACTC CAGCCTAGGC AAAACAAGAG 660
CGAAACACTG TCTCAAAAAT AAATAAAATA TAATAAAATA GAGACTGGGT CTCACTATGT 720
TGCCCAGGCT GGTCTCGAAC TTCTGGGCTC AAGTGATCCA CCCACCTCAG CCTCCTAAAG 780
TGCAATGATT ACAGTCTTGA GCCACTGCAC TCAGCCCATT GTATCATTTG TAATAGCAAA 840
ACACTTAAAA TAATCTAAGT GTCCACCAAT AAAGAACTGG TTAAATACAT TTTGTTATTG 900
AATACCATGT AGTCGTGAAA ACTATGAGGA GGAACTATAC AAGCTGATAT AGAATGATCT 960
CCAAGAGATA CTGTTAAATG AAACAAGGCA AGATTCATAA CAATGATGGT GTACTCCTAT 1020
TAAGGCAAAA TATAAAAATA GACGCAAATA TAAATATATA CTTTCACTTA CTCTGAGAAG 1080
ATAATTGTGG CTAATCTTGG GGAGTGAGGC TGGGGGAGTG AGATTCATCT AATGTATAAG 1140
AGACACATGT TATTACATAT CTGTTTGTAA TTTGAATTAT TTTACCAGGT ACATTTACTA 1200
AATTTTATTT TATTTACTTT TTTTTTTTGA GACAGAGTTT CACTCTTGTT GCCCAGGATG 1260
GAGTGCAGTG GTGCGATCTT GGCTCACTGC AACTTCTGCC TCCTGTGTTC AAGTGATTCT 1320
CCTGCCTCAG CCTCCCGAGT ACTGGGATTA CAGGCACCTG ACACCACGCC CCGCTAATTT 1380
TTTGTATTTT TAGTAGAGGC GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CGAACTCCCA 1440
ACCTCAGGTG ACCTGCCTGC CTTGGCCTCC CAAAGTGCTG 1480
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