| Tag | Content |
|---|
EnhancerAtlas ID | HS112-02996 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr11:63774510-63775940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:63774804-63774822 | GGAAGGAGGGAGGGATGG | + | 6.94 | | SP3 | MA0746.2 | chr11:63774757-63774770 | TGTGGGCGTGGTG | - | 6.21 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65709 | chr11:63774099-63777809 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I064006 | chr11 | 63774214 | 63776295 |
|
Enhancer Sequence | GCTCCCAAGA GTACATGGAA TAAAATCCTC AACTCCAACA AAGCTTTCCT GGACTCTCTG 60
GGGCTCCCTG CAGCCTCCCT CTCAGATGAA TTCACTGCCT CCCGCGCCCC TCCTACTGGT 120
TCCAAACTCT ACCATTCAAA AAATGCGTAC GAGGGCTCGG GGGCGACGTG CCACGTGCCA 180
GCCCTATGCA AGGGCCAGGA GTCCTGTGGC CGCAGCAGTT CTAGGGACGG GACACGCGGC 240
TCTAAGTTGT GGGCGTGGTG AAAAAGGAGA AGGGGAAAAT GGAGCTGGCC CCGAGGAAGG 300
AGGGAGGGAT GGGCGCCGTT CAGAGGATGA GGTGGCCCCT CCGAGGAGGT GGCATTGGAG 360
CAGAGCCCTG AGTAATGAGA AAGAACTGGC TTTGGAAGGA GATGGGGAGG AGAGTCCGGG 420
ATGAGAGTCC GGGCGGAGAG CTCAGGAAGG GCAGAGCCCT GTGGCAGGAA CAGGCCGGCG 480
GGTGAGGCTG GGAGGGAGCG CTGCCTCTAC AGGACCTCCC GGGAGGTGCG AGGAGTCGAG 540
CAATTGGGAA TTGATTCGAG CGCGGTGGGA AGTTTCCATC AGTGAAGGGA CGTGTTCTGG 600
TTCGGCCTCT GGACCCTCTT CTGTTCCCTC TTCTGGACAC GCCCTTCCCT TCTATGCTGA 660
AGCACAGCCC CCTCCCCCCT CGCCCTTTGC CAGACAGCCC CACGCCAGAG GGTCCCGGCA 720
CGCCCACCCT GCACACACAA CACCCACCAG ACTGGCACAG GGACAGGTGC GGGGACTGCC 780
CAGCCCTTCC GGCTGCCTGC TGCTTCTGAG CTCAGCCCTG CTGGGGAGGG GAGGGCCGCA 840
CACAGCCCCG CCTCCAGAGG GCCGAGGCTG GCCACAGGCC ACGGAGGTCA CGTTTATCTG 900
CTCGCAGAGC AAGGCCACGG CTAATCGGAG CGGCCGGAGC TGAGCCTTTT CCTAGCGGCC 960
GCGGGAAGCA ATCACGGATT AGCAGCGGCC GGGCGATGGG AGATAGCGCC AGAGCAGGGC 1020
GCGGAGCGCT TGTGAGCCGG GCAGGAGTCG AGCGCTGAAT ACTTAGAGGC CTGGGCGAAT 1080
CCTCCCGGGC CTGCGGGTCT ACGAACAGAG AACCAGCCAG AGCCAGAGAG AAAGAACGAC 1140
AGGAGAAGGG AGAGGGAGCC AGGGAGAGGC AAAGCGTGGA GGGAGAAATG GAGAAAACGA 1200
GGGAGAGAGG GAGGTGGCAA GAGAAAGAGG TGAGGGAGAG AGGCAGGGTT GTGGGGGAGA 1260
GCGCTCGGCT GGCCCCCAGG GTCCCAGCAT GTGTGTGAGG AGGGACCGGC CCTGGGTGGC 1320
GGCTTCTGAG CAGGTGAGGG AGTCTGCGGT GGGGCCTGGG GAGAGGCGCC CAGGGTTAGG 1380
GTGCGGGCGC GGGACAGGGA GTGTTGTCCA CCTGGCAGAC CTTCACTAAA 1430
|
