| Tag | Content |
|---|
EnhancerAtlas ID | HS060-06832 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr11:109892790-109894000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr11:109893449-109893467 | GATAAGTCCAGACATGTC | + | 6.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTACTAGAT TTTCTAAGGT CACACAGTGA GCAAGTGTTG GAGCTGGGAT TCAGACTGGG 60
ATTCTGTCTA GCTCCAGAGT CTATGCACTG AGCAATTAGG CCATGAATAA ATTTAAGATG 120
CAATTCAGAA GGACAAAGTG GCAGCCAAGA GAGTATGCTG CTTGGGTCTC CATTCAGCTG 180
CAAGGAGTTC AACAGCTTCA GCCTTTATCT GTGCCTTCAG AATCTGCAAA TTTTGAACTG 240
AGGCCATGTT CTTCTTGGTC AGTTTCCCAC CAATGATTAT ATGAGGAAGC CTGCTAAAAG 300
CAGGACATCT CTAACAGGAG TCTTCACTCT GGAGCTCCTT GTTGGCTTGG CAGAGACCAT 360
CAGAGGGGCA CAGCGGCCCC AGGCTCTCCC CACGTGATCC TGCTCCATCT CCCCTTTCCT 420
TCCACAGGAG ACAGATCAGC ATTGCAGTCT GAAGGCTTCT CCTGTTCAAT AATGCTTCCT 480
TGCCATTTTT GCTTTCACAG ATGTCACCCC CTCCTCCAAG AAACTTCTTG CACTGCCATC 540
TCTTCTCAGC ATCTACTTCT CAGAGGAAGT ATCTGGTATT CCCAGTCAAG TATCTGGCTG 600
AGATCTCACC AGTAAGAAAA GAATATGAAA CTTCAGTAAC AAAAATCTGA GCTGCAGGAG 660
ATAAGTCCAG ACATGTCAGA GAGAATTGCT TAGTCAAGGG CAAGCAAGAC ACTAGCTGCC 720
TCACTGTAGC ATTAAACCTT TTGTGTCACA TTGCTTTGCC ACTCTGCTGA CGAAGTCTTC 780
ATCTTCACTC AGGTACTGAT ATTAATCTTA TGCTAGAATA CCTGCTTTCC TTTTGTCATT 840
TTCAACACAG TAAGAGGATG AAATCTGACT TAATTGTATA ATACTGACAT TTTGGCAGAT 900
GCAAATGCTT CCTACTCCCC CAGTTTTACC TGGAAGAGAA TATAAAGCCT CATGCCCCAT 960
GCGACTCCAT GACTGAGCTG ACTTCTTCCC ATTTAAAAGG CAGACAAAGC CCAGTGTGGT 1020
GGCTCACGCC TGTAATTCTA GCACTTTGAG AGGCTGAGGC AGGTGGATCG TTTGAGCTCA 1080
GGAGTTCGAG ACCAGCCTGG ACAACATGGT GAAACCCCAT CTCTACTAAA AATACAAACT 1140
GAGGTGGGAG GATCACCTGA GCCTGGGGAG GTCAAGGCTG CAGTGAGCTG TGATCGCACC 1200
GCTGCACTCC 1210
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