| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36231 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr21:47498550-47499810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr21:47499067-47499085 | GGAAACAAGGAAGGCAGC | + | 6.19 | | MYCN | MA0104.4 | chr21:47499232-47499244 | GGCCACGTGGTC | + | 6.52 | | MYCN | MA0104.4 | chr21:47499232-47499244 | GGCCACGTGGTC | - | 6.52 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02356 | chr21:47498343-47500268 | Astrocytes | | SE_26913 | chr21:47498605-47499444 | Esophagus | | SE_38911 | chr21:47498469-47500136 | IMR90 | | SE_44138 | chr21:47497366-47504865 | NHDF-Ad | | SE_44834 | chr21:47498418-47501089 | NHLF | | SE_45632 | chr21:47498053-47502099 | Osteoblasts | | SE_56017 | chr21:47498590-47499871 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 47498553 | 47498697 | | chr21 | 47499343 | 47499535 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I046078 | chr21 | 47498343 | 47504493 |
|
Enhancer Sequence | GTGGGAAAGA AAGACGTATT CCGGGGTTTG TGCATCACAG GCTTAGGCTC TGAGGGGAGT 60
GGAAGTACCA GGGCGGAGAG GAACCTTCAG CAAAGATCCC ACGTGGCAGA GGCTGAGCTG 120
GAGAGGGTGA CCTCAGCAGG GAAGTGAGGA GAGCACAGAG CAGCCAACCA GTTCCTGGCA 180
GCTTTGGGAC CGTGTCTTCT GGGGACTGTG GCCAGGTTCA GGCTCAGCCC TCACCCTTGG 240
TGGTGACTCC GAGGCCGGCA GAGCCCCAAG TCAGCCTGTC CTGGGCAGGC ACAAGGGTCC 300
CACAGCAGGG TCACCCGGAG TCCCCAAGCT GGGCACCCTA AGGGGTGTCA CCAGAGGAAA 360
CACTTGGGTC TGTGGCTGAG GCTGAGGACC TGGCTGGGCA GAGGCCCCCA TGGCCTTCAT 420
GCCTCTGAGA AAGGGTCAGA AAACTCCTGA TGATGGAGGT TAAACAGCCG TGGTCCCTGG 480
GGCATGGAGG CCTGAATGCC ACTGAGCCAA GTTATGTGGA AACAAGGAAG GCAGCATCCA 540
GCACCACTGC CCATGGGAGA CTGTGGGCGT GACCAGGTCC TGCAGGGTTG CAGAGGATGC 600
CCAGGGGACC GGCAGCCCGG GGCTTGCAGG AGGGACCCCA GGCCCACTGA GCTGCAACTT 660
ATCAATTAAA CCCAAGGATT CAGGCCACGT GGTCCCAGAT GTGAAGTCGA GCCCCAAAGC 720
CACTATCAGA CTTTGGGATC CCAGCCAGGT CACCGGCCTC CCTGCTCCCG GCTCCCTCCT 780
GGTCCAACAT GGACTGGGGG TCTGAGGAGT CCACGAAGCT ATGTGCTCGC TGCTCAGACA 840
CTCACCCCCA CACGTGCTGT CACTGGCGGC TGGGCTCATA ATTGGAAACA GACCCATGTG 900
ACTCAGAGGA AGCCAGCACT GCCCCAGCTC ACGCAGGCCC TCCTCGGAGC TTTAACAAGG 960
GGCTAGCTTC CTGTGAGCCC CACTGTGTCC CACTGACATG TCAGCCACAC CGCTGAGTTC 1020
ATCCAGCCAG GGTGTCTTGG AAGGTTCTGT TCCCACGCAC GTAGCCAACA GCACCAGGCT 1080
ACACACACAC GTGTGGACAC ACATACACAC ACACACATGT GCGCACACAC ATCCACACGC 1140
ACATGCACAC ACACGTGCAT GCACATACAC ACCCACACAC GTGCACACAC ACGCGTGTAC 1200
ACTCGTACAC GCACATGGAC ACACACACGT ACACACATAC ACATGCACAC ATCCGTGGAC 1260
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