| Tag | Content |
|---|
EnhancerAtlas ID | HS082-14866 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr17:41772460-41775030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr17:41774026-41774038 | GCTATTTATAGC | - | 6.32 | | MEF2B | MA0660.1 | chr17:41774026-41774038 | GCTATTTATAGC | - | 7.22 | | POU4F2 | MA0683.1 | chr17:41774511-41774527 | GTGCATAATAAATGTG | + | 6.77 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGACATAGT CTCGCTCTGT TGCCCAGGCT GGAGTGCAAT GGTGCGACCT CGGCTCACTG 60
CAACCTCCAT CTCCCGGATT CAAACAATTC TCCTGCCTCA GCCTTCTGAG TAGCTGGGAT 120
TACAGGTGCC TGTCACCATG GCCAGCTAGT TTTTGTATTT TTAGTAGAGA CTGGGTTTCA 180
CCATGTTGGC CAGGGTGGTC TCAAACTCCT GACCTCGTGA TCTGCCCGCT TTGGCCTCCC 240
AAAGGAAGCT TTTATTTTTA TTATAGTTTT ACATAAGGAT AAATTCAGCC TTAGTGAAGG 300
GAAGTGACTT GCCCAAGATC ATACAGTGAG ACTGCTGGAT CTGGGGCTCT ACTTCAGAAT 360
TTTTTTTTGA GATGGAGTTT CACTCTGTTG CCCAGGCTGG AGTGCAGTGG CACAATCTCG 420
GCTCACTGCA ACCTCCACCT CCCGGGTTCA AGCGATTCTC CTGCCTCAGC ATCCCTGATA 480
GCTGGGACTA CAGGCTCCCA CCACCACGCC CAGCTAATTT TTATATTTTG AGTAGAGACA 540
GGGTTTCACC ATGTTGGCCA GGCTGGTCTC AACCTGCCTG GCCTCCCAGA GTGCTGAGAT 600
TACAGGTGTG AGCCACCACG CCAGTCTACT GCCATTGTCC ATGATTTTTC CTACAGGGAA 660
AATCACAATC CCAGAAGATA AGACAAAGAA CAGTAAAAGG TGGCTTTTGA GGCAGTGAGT 720
TCTACCTGAA GGTGGGAACA GCCCAGAGTG TCTGGGGACA GAGTGGTAAA TTCTAATCAA 780
GCCTTCCCAT GGCTTTGTGG ATGAGGATGA GTTTCTACCC TGAAGCTCGG CCTGTTCAGC 840
CATAAAATCA GGATAATGGT GGCTGTGCCT CCTTAGAGTA GAATGAGAAT CAGAGCAGAA 900
CAAGGGAAAG CTGCAGTGAC TTGTCAGGTG TCAACCTTCA GCATGATGGG AGAGCCATGG 960
GACCCTTCCC CTTTCCCTAA GAGAGCCAGC CCTCACAGCA GGCCTGGGAT CCAATGCCCA 1020
GCACCCAGCT GGGAGCCCAG GGACCTTGGC CAAAATCTGG TTCTGCTTCA ACTTGGTGCC 1080
CGGCCTTTGT CAAGTCACTT CCTCATTTGC AAACTGGGAG AGTTTGGATG AAACTATTGA 1140
ATGAAATTAT TTTGGGGGTT TCTTTCTGGC TCTCACAGTC CTCGCATGCT CACCATGTTC 1200
CCTTCAATTT CATTAGCACA GCCCAACAAA GGGTTAAGCA GTGGCAGTTC CTCTCGTTCT 1260
TTGGTTAGGA CAGGAAGGTC AGGGGTGAGG CCAATACAAG AGGTAGCCGC CACAGCTGAT 1320
GCTGGAAATG ACAATAGTTC TTTCCTAGAC TCATATTTGT CCCCTCTCCC TGAAGCTTTG 1380
CCTGCAGTGC CCTTGTAAAG AAGTTGGCAA GAAGCAGGAG TGAGGCTCAG CCCCTCTCTG 1440
AAATGGATAC GCCGGTTGCT CCCCCTCATG GCTGGTCTCA TTTGCCTTCT TCATTTTTAG 1500
ACACATTCCA AACTTTTCAG CAAATTATAG TGTTTGCCAA CTGGCCGTCT GGGGCCCAGG 1560
AGAGATGCTA TTTATAGCGA TGCTGGGATG CTGCCATCCC AGAGCAGCCT GGTAAGAAAC 1620
GGAGCCAGAG TGCCTGGGAG TGGCGTCCTG CACCCTGGGG AGAGGCCAGG GCCCTGGAGC 1680
AGGGTGGCAA AGCTGGTGGC CCGTGGCAAG GACCACTGGC ACATCCCCTG CCTGCCTGGG 1740
CCCTGGGGTC TGTGCCCATA CCCCACACGG GGGGCTGCTT CCGTGCTCCT TGGAGAGACG 1800
ATGGTGCTGT GGGGCCACTG AGCACAGTAA AGGCTAAGAC CCACCATAGG TCAGCCCTTG 1860
CTCATGCTGA CTGTTGCCCC ATTTCCCTTC ATTCTCTCAC TCGTTCATTC CTCAGAATCT 1920
GCATCCTGGT TTTGTCACTA CCTGGAGTTG TAAAGATACC ACCAAGCTCA CCTTGTGGTG 1980
TGAGCCTTGA TTTTCCCCAT CTGTGTAAAG GGTGGATCTG AGCTCCAAAG TTCCTTCTAG 2040
TCATATGCAG AGTGCATAAT AAATGTGTTT GTATTCCCAC TGTGCTCAGT GGGCACTGGG 2100
GCATGCAGAA GAGAAATTGG AATAAATGTG ACCCTTGTCC TCCAGAGGCT CAGTACCAGA 2160
CTGGAACCAG GACCCAGATG AGGGGCCTAC CCAGAGAGGG CAGCGTGCTC TCCTATTTGT 2220
GTTAGGCGTT ACCATTTACA AAGGGCTTTA CGGCTTTGAA GGTCCCCACA ACGCCCTGAG 2280
GAGGTGAAGT GTGGCAATGC CCGTTCACTT GGGAAAATAC TGCATCTCAG AGAGACCAAG 2340
GGACTCGCTT AAGGTCACAC AGATACAGTA AGTAAGTAGG GAAAGAGCTG GGGCCTCTGG 2400
GCTCCTTTTC CGGGGCTCTG GCCTCGGTTT TAACCCGTTC TCCTAGACCT CTCAGTCTCT 2460
GGGCCTCCCC TCTGTGTTCC CCACCCCCAC TTTCCATCAA GAGCTCAGTT CTCTTAAGTT 2520
CTATATTCTC TCTTCCCCAC CCCTAGAAAT CTCTGCCCGC TTCCAGAAAA 2570
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