Tag | Content |
---|
EnhancerAtlas ID | HS184-17931 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:25095810-25097160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:25096982-25097000 | CCTTGCTCGGTTCCTTCC | - | 6.1 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 25096281 | 25096800 | chr20 | 25096520 | 25097000 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH20I025115 | chr20 | 25096021 | 25096170 | GH20I025116 | chr20 | 25096741 | 25098307 |
|
Enhancer Sequence | ATGCATGACA GATGGACAGA AAGACAGATA CAGCTATATA CACATATACA TAGGAATTGA 60 CTTTATAGTT ATGCTTCTGA CAGATTTAGC ACAGCCTCTC CTGATGCAAG TGGGAGGAAT 120 TAATCCTGCT CAAATGAAGC CGGTTTTCTC AAATTCAGGG ACTTGATTCC TAGATTATGC 180 TTTAGGAAGA TGTTGATCCC GCCCATGTAT ACAGTATGTG TTTGGAACTG CAGTGTAATC 240 CAGGCTTACA GCATGAGCGT TAATGATTGC TAAGTGCTTT ATTTACAGTA CATTCCACAG 300 GGCACTTCCT GAGAGAAACT GGGTAGAAAT GGCTCCTGAC TTATAACAGG ATGCTTGTGC 360 CCAAGTTTTT TGTGTTTTTT GTTTGTTTTT GAAACAGAGT CTCACTCTGT CGCCCAGGCT 420 AGAATGCTGT GGCACAATCT TGGCTCACTG CAACCTCTGC CTCCCCGGTT CAAGCAATTC 480 TCCTGCCTCA GCCTCCCGAG TAACTGGGAT TACAGGCGCC CACCACTATG CCCAGCTAAT 540 TCCAAGTTCT AAAATTCTTT TTTACATCTT ATGTTTTATG AATTTCCTCC AGTACACTTT 600 ATGCAAAAGT CAGTAAAAAT ATTTCTCCTA TAAGTCTAAA CAAATGTTTA AAAATATGTA 660 AGTTAGGAAG TTATTTCCAA CACGCATATT CTTTTCACAT GCAGAAGTAA TGGTGAGAAT 720 TTTTCATATC CTTTGCAGCA GACTCCCGGC CCCGGGGCTG GGCCCTCAGC AAGCTCATTC 780 CTGTGGCTGG GAAGGCTGGG GAGGCAGAGC TGGCTTCCTA GCAGCCTGGG GTTTCCTCGG 840 GTGGTTTTTG TGCAAGTTAA ATATGCTAAG AAAGTTTGGT TGTAGGATCA GTGCCTGACC 900 AGATGCCTTT GCCTTTTACT GGCTGGTGCT GCCACACACA CACACACACA CACACACACA 960 CACACACACA CACCCCTGAT GCTGTGAGAC TTGGCAGCTA CAGGCTCACT GGGCATCCTT 1020 CCCTGGAGAA CTGCCCGAGG CTGGCAGAAC CACCTGGCTC CAAAATGCCT GGAGGCCCAG 1080 CTTCCTCCAC TCACCCTCAG CTGACCCGAT GGGTCCTCCG CTGTGCCCCT TCCTCAAGGC 1140 AGGACTTGCT GTGGACAATT CATCCCTCAC ATCCTTGCTC GGTTCCTTCC ACTCTCCTAT 1200 CCAGCTTTGC TCACTCCCTT CTCCTCAATA ACACACAAGC ACCAAATCCC TGCCTTAGGA 1260 TCTGCTTCCA GGAGACCACC TAAGCCAAGT GGTCATTTGG CTTAGTCAAC CTCCAAGACT 1320 GGCATTTATA TGGCTGTAAC ACGTAGAACT 1350
|