Tag | Content |
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EnhancerAtlas ID | HS051-15513 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:71227860-71228940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:71228406-71228425 | TGCTGCCCTCTAGTGGCGA | - | 7.81 | RREB1 | MA0073.1 | chr2:71228556-71228576 | CCACCCACCACACACACACA | + | 6.38 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I071000 | chr2 | 71227931 | 71229948 |
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Enhancer Sequence | AGAAACCAAG GCACGGAGAG GTTCAATATC TTGTCCAAAG TCATACCACT AATATTTTAA 60 GCAGCCAGGG GTCAAACCGG GGCAGGCTGG CTCCGGAGTC CACATGGTTT TCTCTGGTCT 120 TTCTGAGTTG AGTCACCTGA CTTTGCAGTT AGGGTGATTC TGCCTGCCTT GTCATCAGGT 180 GCCATTTGGC CAGTGGGCTG GGTCCTGCCT CATCTCCCTG CAGGCTGCCT GGTCCCCCGG 240 GCTTTTCCTC TTCTCCCCTG CCTTTATCCT TGCAGGAACA AATGAATACA CCTCAGGGTT 300 CTGGCTTTGA CCACCCCTGG TCCCCTCCAC TGTCTTCACC CACTCCCCTT CTCATTCTAA 360 CAGACTTACA CATTCACTAT GCCTGAGGCC AAGGACATCC TTAGTAGGAT CTGTGGTCCC 420 AGTGGTCCAC CCACACGCTG GGGACCTGCA CATCCCCAGG GGCTAGGAAG GTGCGGGGAG 480 GTGGAAGTAG GAGGCGGTAC GGCCGGAAGT CGGCCGCCAA AGTTCCCCTT GCCGGGCTGT 540 GTTGGCTGCT GCCCTCTAGT GGCGACCAGA GGAGCTGGCG AGGACCGAAG CCAGGTTCAT 600 CGCTTATGGA AAGCAGTTTT GAGAGACAGT GGGGACCCCA CTACCCGACT CATGAAGGCC 660 AGGTGGGCAG GCCCCGAGAG TACACACAGC CGACACCCAC CCACCACACA CACACAGTAC 720 ACAAAATTGT AGACAGGGTC CACCTCGGCA TCAGGGCTCC TGCTGCCCCG GCATGGTCTG 780 GCTACAGACG ATGGTTGTTG TGTGAGAGAC TGTGAGAGAC ACTGTGAAAT CAGACATGGC 840 AGAGACAGGC CTGGAGGCCC AGGGCCCTCC CTCTGCCTAG TCTTCTCCTC CCCCGGTGTG 900 GCTCTTACCT GGACCTGAAC TCCTTCCCCA CCAGCTCCCC AGGCCTCCCA GGAGCACAGC 960 TTTGGGGTAG GAAGAGCTGA GGAGAGAGGT TACCGCCCGC CCCACTGCAC CCTAACACAT 1020 GCCATCCACC ACACGATGTC CCCTCTTTAA GGTGCCACAT GCTGGGGGAA ATTTTTCCTG 1080
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