| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18149 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr21:46975260-46976450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr21:46975556-46975566 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr21:46975561-46975571 | GGGGCGGGGC | - | 6.02 | | NR2C2 | MA0504.1 | chr21:46975939-46975954 | GAAGGTCGGAGGTCA | + | 6.24 | | Nr2f6 | MA0677.1 | chr21:46975947-46975961 | GAGGTCACAGGTCA | + | 6.51 | | RREB1 | MA0073.1 | chr21:46975336-46975356 | CCGTGGGGGGTGTTGGGGGC | - | 6 | | Rxra | MA0512.2 | chr21:46975947-46975961 | GAGGTCACAGGTCA | + | 6.26 | | TFAP2A | MA0003.3 | chr21:46975586-46975597 | TGCCTGAGGCT | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31863 | chr21:46975252-46976414 | Gastric |
|
| | 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 |
| GH21I045548 | chr21 | 46968529 | 46977419 |
|
Enhancer Sequence | CGCTGCAGGT GGGGGTGGGG GTTGCAGGGG CGGCGGGGAC AGTATGGGAG GCAGGGGCGG 60
TGTGGAGAGC TGGGGGCCGT GGGGGGTGTT GGGGGCGGGA GGGGGATGGG GGAGGTTGTG 120
GGGGGAAGGG GAACCGGCTT GGGTGGCCAT GCAGGCGACG CGGGTTGCAG GGAACGGAGG 180
TGCAGGGGGC GGCGGCGGGG GCGGCGGCGA AAGGGGACGG GCTTGCGTGG CCCCGCGCGG 240
GGGCTAAGGG GCTGCAGGCC AACCCACCGT CCCGGGCACT TGGGACTCAG GAGGGCGGGG 300
CGGGGCGGGG CGGCCCGCGT GGGGAGTGCC TGAGGCTGGC CTAGGCCCTG GGACCGTAGC 360
CTCCCGAGCA GGGTGGGCTC CACGCGAACG GCGGGCGCTG GCAGAAAGCG ACCCACGCAG 420
AGTTCCGCGC CAGCCGAGGG GCCCGGCTGC CGCCCATGCG CGGTCCTGGA GGTGCCGGGA 480
GGGGGTCGCG GACCCTGAGG CAGGATCCAC GTGGTCCCTG CGGGCCCAGT GAGTGACATC 540
ACCGCGACGC TGCGCATGGA GCAAGCTCTA CACCCGGGAG ATGGCCACGG TGCGCATGCA 600
GCAAGGTCTA CTCCCGCGAG GTGACCACGG GACAGACGAT CCTCTGAGGT TTCCAGGAAG 660
ACCCCCGCCC TAATCCTCTG AAGGTCGGAG GTCACAGGTC AAAGCCGAGA ACAGAAGCTG 720
GGGTGGGGCA CACAGAGGTG GAAAGAGGGG CCTGAGCATC GGGCGGCCAC CAGCAGGGTC 780
CCCTCCTGGC CACAAGGACG CTCCCGTTCC AGTCCCCGGA AGAGGGTGGC TGCAGCCACC 840
CCGGGGATGA CCAGCAGAGG TCCTCACGGC CTGCGGCCCG GGGAGACCTG AGACTCCTAA 900
GCTGAGCACG TCAGCGTCTC TACCTCCACC GCAGACAGAA AGACCGGGCG GACCCAAGAC 960
TGCAAGCTCA AGCCCTGGCG GCAGGGCAGC GGGGCCTGTG AGGGCCGAGG GTGGACGCTG 1020
CTCTGAGCCA GACCCGCTCG TCAGCAGCTC GGCCTCCCCC GCTGCTCCCC ACCAGCGCCC 1080
GGGCTTGGGT GTTTGGTGCT TCCAACTTTT CAAGAGAAGC TTGAAATCTG TAATTCTTAT 1140
GTGAAATCCT GCCTTTCTTA ACTAATTAAA GACTTAAAAT TAGCTAGTTA 1190
|
