| Tag | Content |
|---|
EnhancerAtlas ID | HS139-56947 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr9:120524960-120526480 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr9:120525705-120525719 | TGGAAATGAGTCAT | + | 6.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGATACCTA CTTGCATAAC AGATTTTGGG TGAAGGTGGT CTGGAGTAAA GAAGCAGGAG 60
AGGCCTTTAG AGAGAACTTT GAATTCTAAG CTGAAGCCTT TCTCCCAAGG TCGTGAGATG 120
CTATTAAAGG ATTGAGAGCA GTGAGTGTAG ATGAATAATT CTGCATTTTA GAACCATTAC 180
TTTGGAGCCT GTTTTGGAAG GGCAGGACTG GAGGCAGAGA TATGGATGGA GGATTGTTCA 240
ATATTCTAAA AGAAGGGTGA TGGTAGTGTG ATCCAGGAGC ATGCGAGTGG GCCTTTGGAG 300
AGATGCCAAA GCAAAAGAAA GAAGGAAACT TAGTGGCTGG CTAAGAGGGA TAAAGGTGGG 360
GAAGAAATCT GAATGAACAC CTTGGTTTCT GACTTGGGTG ACAGTTCATG GTGGCACCCC 420
ACATTCAAAT AGAATTAAAA GAGTGCAGAA GGAGGGACAG TCTCTTCTCC CTCTGGAGAT 480
GGGATTTCTG CAGGGAGGAC ACTGGGTCCT GTGACACTAG CTGTGCAGGT CACAGGCCTG 540
CAGGAGCATT GAGCCAAGCA GGTCATTACA GGCATATCCA CATCTGTTAT AAAAACTGAA 600
CTCTAATCGT GCCAGACCCA CTCTGGCATA ATAAGTGTGG TTTTTAACAT AATGCACTGC 660
TGGAGCGAAG TTGTCAGAAA AGCAGGAGGC GGAGGAGGTA ATCTGTGAGA CTTCAAAAAA 720
GAAGATTGAA GCCATTTTAT GTGGCTGGAA ATGAGTCATT TGTCAGCAAT GCCAATGTGC 780
TGTCAGCTTT GGAGGAGAGA TGACGGGGCA CCCTGGGGGG AGGGCTGGTG AAAGTGTCAA 840
CCTTCAGTCA CCAGAGGCCA TGTGTGGGGT AAAAAGTGTC AGTCACATCA CATCCCTGTC 900
CTGACCTGGG TTAGAGGAAA ACCAGGGTCA CAGCAGAGCA TTAGCCTTGT AACCAAGGAA 960
CCTTGTAACC CTCCTCTCTC AGGAAGGAAC TGATGTGCTC AGCGTTCTCA AAGACTGTTC 1020
AGAGCTTTAA TTCCTCGGGG CATGTGCACT TTAAAAGAAG AGTGGGAGTG CAACACTTAG 1080
GAAGAAGAAA CTAAGGGGTA AGAGTGGATT GGTGGCAGAA AGGAGGAGAG ATTTCGAGCA 1140
AGGACTTGCC TAAGGTCACT TACATAGGTG AATACCCCTT CTCTCTACCT AGTTGCCAAG 1200
TCCAGGGTTA TCTCTGGGTC CTAATAGCTT GGAAGCCATT CCTGGGAGTG ACAACCCATT 1260
CTAAATGGAG TGATCCCTGC TTTGTATGTT ATTGCATTAC CTGACACTCC CCTACCCCCA 1320
TCATGCCAGT ATCGATCACT TGGATACTTA CTTGGGGTAC AGCAGCAGAT CATCCTAACT 1380
GGTTCAGCCT TCATTGCTCT GCTCTCATCC ATTTTTTTTT TTTTTTGAGG CCATAGTGAC 1440
CATCTTAACT TGAATTGAGT CTTCGCCTTT CCCTGTTCTT TGTGTCCTCC CAAGCTACCT 1500
GGCTTTGGTC TCTAACAACC 1520
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