| Tag | Content |
|---|
EnhancerAtlas ID | HS089-02494 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr11:61361220-61362890 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:61362212-61362232 | CGGGGGAGGGTGGGGTGGGG | - | 6.7 |
| | | 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 |
| GH11I061594 | chr11 | 61362418 | 61364149 |
| Enhancer Sequence | CTCACTGCAG TCTTAACGTC CTGGGCTTGA GCTATCCTCC CACCTCCCGC CTTAGCCTCC 60
TGAGTAGCTG AGATTTCAGA TGTGTGCCGC CAAGCCTGGC TAAATTTTAA TTTTTTTTTT 120
TTTTTTTGAG ACAGAGTCTC GCTCTGTCAC CCAGGCTGGA GTGCAATGGT GTGATCTGGG 180
CTCACTGCAA CCTCCGCCTC CCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCGAGTAA 240
CTGGGCCTAC AGGCATGTGC CACCACACCC AGCTAATTTT TTGTATTTTT AGTAGAGACG 300
GGGTTTCACA GTGTTAGCCA GGATGGTCTT GATCTGCTGA CCTCGTGATC CGCCCGCCTC 360
AGCCTCCCAA AGTGCTGGGA TTACAGACGT GAGCCACCGC GCCCAGCCTT AACAATTTTT 420
TTTGTAGAGA CAGGGTCTCA CTGTGTTGCC CAGGCTGGTC TCGGACTCCA GGCTTCCAAT 480
CCTCCTGCCT CGGCCTCCCA AATCGTTGGG CTTACAGGTA TCAGCCAACA TGCCTGGCCC 540
ATAGGAGTAT TTTTGATAGA GTGGTGGGGA TGAAAGCCAG ATTGGAGTGG GTTTAAGAGA 600
GAACAGGAGG AGAAGAACTG ATGATAGTGG ATAGAGACAA CTCTGGGAGG AATTTTGTTG 660
CAAAGGGGAA CAAGGAATTA GGTGGCAGCT GCAGGGGAAG CAGGATCAAG AGCAGGTATG 720
TGTAAGATGG GAGGAAAAAC AGCCACTGAC AGGAATGGTC CGGTGAAGAG GGACGGGATG 780
ACTTGCTGAT CAGAGGGACT GGGCTCTGGT GCCCGCCTGG GGTGGTGGGT GAGGGCAGGC 840
GTGGGCAGTC ATCTCTCCTA GGACTCGGGG AGACAATGTG TGGGTGCAGA GGCTGGTGGG 900
GGCGGATGTG TCCGTGTAAA TCTGGAAGTA CTTCTGAGAG ACTGGATTGT CTTCAGGGAG 960
TGAGAAACAA GGTCAACAGC TGAGAGTGAG GACGGGGGAG GGTGGGGTGG GGTTTGAGGA 1020
GAGGAGATCG TGAGAAAGCA TGAATCGCCC ACGAACAAGG GAGGGTGAAC AGACTCAGTG 1080
GTAAGTGTGA AGAATCGCCA GCCGTGAGCC TTTCTGCCCC ACTCGGGCTG GGGTCAGCTG 1140
CCCACCTCCG GGCTCCCGGG GCTCCCTGAC CCCACTGAGG TTTAAGCCTT TACTGCTGTA 1200
GGAAAGGGTT ACCAGCAAAC CCCGTGCAGT CAGGCAGCCA GCATTTGAAT TCTCCTCCCG 1260
TGCTCACTGG CTGTGTAACC TGGGCAAAGT TTTTGTTTGT TTTCGTTAAT TGTCCGCATG 1320
CCTCAGTCTT CTCATCTGTA AAGTAGGGGC GGAAGTAGGA GGAAGCACTC TGTGTTATTG 1380
CTATCCTCTA CTCTGTTGTT GCTAGTTTGT ACTGAGGAGG GCTCAGTGAA TGCAGAGTGA 1440
AGGGTGAATG AGGGGAGGGG AGTTTGCTTT GGGCCCCCAC ATGCCAAGGA GTGGGCAGAG 1500
GAGGGCAGGT GTCACAGCTC TGCCCCTGCG CACGGACGAC TCCGACTCTT TAACCCCAGG 1560
GCTCAGCTCC CATCACGTGA ACTGGGATCC CTGAGGAAGC TCTCAGGTGG GCGGCCACCA 1620
GCTGAGAACA GACCTCCCAG TGCAGCCCAG GACAGTCCCT AGCACAGCCC 1670
|
| |
|
|
|
