| Tag | Content |
|---|
EnhancerAtlas ID | HS043-44413 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr9:133852210-133854530 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr9:133853870-133853884 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATAACCTAC ACACATCCTC CCGTGTACTT TAAATCATCT GTAGATTACT TATAATACCT 60
AATGCAATGT AAGTGCTATG TAAATAGTTG TTACATTGTA TTGTTTAGGG GAATAATGAC 120
AAGAAAAAAG TCTCTACATA TTCAGTACAG GTACAAACCT TTTTAAAAAA TATTTTCAAT 180
CCGAGGTTGG TTGAATCCAC AGATGCAGAA CCCATGGATA TGAAGGGCCG ACTGTATTCA 240
CTGAAGACCT CCTTTGGGCC AGGTGCTGGG CGAGGCCCCT GGGATACAAA ATAATAAGGC 300
AAATCCCCCG GCATGAGGCT GCTGTCCTAG TGGGAGAGAT GAGCCTTGAA CAGGGAAATA 360
ACAGCAAGCT TAACACACGA GGGCTGGGGC TGGTCAGGGG CTGCAGCATC TGGGGCAGGT 420
GTGAGGGGAG GCGGGGTTCA CACGCACACA CAGGCATGCA TGCATGCGCA CATACATGCA 480
CACGCGCGCG CACACACACA CACACACACA CACACACACA CACACAGAGT TCGTGGCTGG 540
ACCCCCGCGG CAGTAGCCTC TTAGGTGTCT GAGATGAGGT CCGAAGCTGA GGTGTGAATG 600
AGCTGGGCTA AAATTGCAGG GAAGAGTGTT CCGGGCAGCA GGAACAGCCT TGCGAGGCCT 660
GCAACAGAAT GAGCACGGTG TCTGAGGGAC TGAAAGAGCC AGTGTGGCTG GAGCATCTGG 720
CCCAAAATGA AGAGTGCTGC GAGTGAGGTG GAGAGGCCCG CGGCGGCCAA AGCAGGCGGA 780
CCTGGCGAGC CACGCCAGGG CTCTTTCACC AGGGGCGCTT CGGAGCCAGC AACAGGCGTT 840
GGACAGGAGA CGGTGTAAGC CGACGCACAT TTGGGAAAGA TGGACTGGCT CCTGGATGGA 900
CAGTGGATTT GTAGGGAGTA GTGGAGGGAG GAGGAGTCCT CGGAAAGACC AGGGCAGCCA 960
CCCCAAGGCC CGGAGGTGTG AGGCTGAGCG CACGGGGGAG AGCAGAGGGC TCTGGGAGAG 1020
GCCTAGGTGT CGCTTGAGGG GACGTGTTGA CAGATTGGCC TTTTGAAAAA GTCAGCTGGC 1080
CCCAGGGATG GAAGGAAGCT GGTGCCAGGA GGTGGTATAG GGGCTGGGTC CAACTCTGGC 1140
AGCCTGAGCT GGGTGAAGAG ACTTGCCCTG TGTCCCAGCT GCCCCATTTC CAAGCAGCAT 1200
GACCTCAGAA AGGTCGCTTT GCGCGTCTGG CCCTGACTGT GTGCTTATCT GTTAAATGCT 1260
CGATCGGCAC GAGAGGATGG GTAACAACCC CCGAATCTCA CGGCCTGGAA AGCGCAAGTT 1320
TGTTCTTCTC TCACACGGTA CACCCATCCC CCACGGGCTC TGGAAACCAG GCTGACAGGA 1380
GCCAGAACAC GTGGAGGGAG AGCCAGGGGT TCCCACATTT TTTTTTTTTT TTTTTGAAAC 1440
AGAGTCTCAC TCTGTAGCCC AGGCTGGAGT GCAGCGGTAC CATCTCAGCT CACTGCAACC 1500
TCCGCCTCCT GAGTTAAAGC AATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG 1560
GCAGGTGCCA CCACGCCCGG CTAATTTTTT GTATTTTTGG TAGAGATGGG ATTTCACCGT 1620
GTTAGCCCGG AGGGTCTCGA TCTCCTGACC TCGTGATCCA CCCGCCTCGG CCTCCCAAAG 1680
TGCTGGGATT ACAGGCATGA GCCACCGCAC CCAGCTAATT GGTTCCCACA CCTGAACGCA 1740
GCCCACATCC CTCCCTGTCT GGATTCCTTG GCTGGAGGGA GCCATAGGGC CACACCTCAC 1800
TCCAAGGGGG ACAGGCAGCG AGAGCCACCG GACATGGGTT CAGTGACGTC CACTTCACAG 1860
GGTGCTGTGC AGAGTGCGGT CAGTGAGGTG CTGCGGGAAG AGATGACTGT GCAGAGTTGA 1920
TGCTCGGTAC AGGGCAGAAA GGATGATCCC AGGAACGCAT CGCTGGACCC GCCTCCCCTT 1980
CCTGGACATC TCCCCAAAGG GGAGTGTGAT CTGAGTCCGT GTTCCCCAAA CCTCCATCAC 2040
CTGCCAGACC CATGGGCCAA TAAGAATCAG TCACAGAGGC TGGGCGCGGT GGCTCACGCC 2100
TGTAATCCCA GCACTTTGGG AGGCCAAGGC GGGCGGATCA CGAGGTCAGG AGATCGAGAC 2160
CATCCTGGCT AACACAGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT TAGCCGGGCG 2220
TGGTGGCGGG TGCCTGTAGT CTCAGCTACT CGGGAGGCTG AGGCAGGAGA ATGGTGTGTA 2280
CCTGGTAGGC GGAGCTTGCA GTGAGCTGAG ATCGTGCCAC 2320
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