Tag | Content |
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EnhancerAtlas ID | HS051-21553 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:317050-318050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr5:317691-317706 | CGACCACCCACCAGG | + | 6.56 | RREB1 | MA0073.1 | chr5:317594-317614 | GGTTTGGGGGTGGAGGGGGT | - | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 317147 | 317733 | chr5 | 317573 | 317753 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I000317 | chr5 | 316865 | 317843 |
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Enhancer Sequence | ACATTTCCCC GGGGAGCTCC CAGCCATCAG AAGTCAAGGG AGGGAGGCGG TGAGGAGCCT 60 CTCGAAGCAG AAGGTGTGGA GGGGGGACTC CCCTGCTCTC CTGGCCGGAG TCACTGATAC 120 AAAACTGGGG GTCCCTGGAG GGCAGTGAGC TCACGAGTTG TGGTGGATTC CTTGTGGAGG 180 GGGTGCCAAC CCGCAGGGAA GCAGGGCTGC CGTGCCCCCT GCCCAGCCAC ACTGCCAGCA 240 CAGACCCCAT CCTCAGGCGC CTGCAGGGAG GCCACCCACG CCTTCCTGGG TGAGGGAAGC 300 CCCTGAGCTA AACCTCACTG CACTCTGAGG CCCCAAGGGC CAGGCAGCTG CACACAGCCT 360 GGGCCACGTG GGGGCAGTGC GGCTGCACCA CGGAGCTCTC GGGAGCTGCT GACTGACCGG 420 GAGGACCTGC CCGACACAGC CATGGGATTT ATAGCCGCAG AGAGAAGACT ACAGAGAGAC 480 GGGCCTTCGC CCTTTCAGCT CTCCCTTGTC AGGCAGGCTG TGCCCTGTGA CCCTTCAGAG 540 CCTGGGTTTG GGGGTGGAGG GGGTGGACAG CTGACCAGGT GCCTGGCGCA GGCCCAGTGT 600 GGTGAGGCTG GGTCGCGGAG GCCAGGCCAG GCCAGCGGCC ACGACCACCC ACCAGGGACC 660 CTCAGCGTCA CGACCCCGGT CCCAAGACCC AAGACAGCAG GACATGGGGG CACAGCCATC 720 TCTGGGGGCC TCTCCTTCCC CCCGCTCTGG GTCCTCAGTC ATCAGTGCAG ACATGGAGGT 780 GCAGGTGCAC GCCGTACACC CTCACCTGGG GCCCCTGGCC CATGCCTCCC CACCCTCCCT 840 ACCCTGATCT CCCCCCACAA CCCTACACCT CCCCGGACAA CCCTGCACCT CCCCCAACAG 900 CCACCCTGCA CCTCCCCGCC ACAACCCTGC ACCTCCCCCA ACAACCCTTC AACTCCCCTC 960 TCACCTTGCA CCTGCCCCTC ACCCTGCACC TCCCCCCATC 1000
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