| Tag | Content |
|---|
EnhancerAtlas ID | HS138-25175 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr21:47498300-47499990 |
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: 3 | Chromosome | Start | End |
| chr21 | 47498553 | 47498697 | | chr21 | 47499343 | 47499535 | | chr21 | 47498460 | 47498558 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I046078 | chr21 | 47498343 | 47504493 |
|
Enhancer Sequence | CGTCCACACC AGGTGAGACG GGGGGTCCAG AGAGACGACG GGCTTGAGGG GTCCTCACCC 60
TGCACCTGCA GCACCAAAAA CTCACCGAGG CCCTCAGGGT CCTCCTTCCC GCACCAGCGG 120
TTCTCTTGCA CTTTCTCCTC ACTCGGGACT CAAGGGGCCA CCCAGAGCAG CCACCGCAGG 180
CGCCCTGCAT GGCTAGAGGG GCCGCCAGGG TCCATGCTCC CGGAGCCTTC TCAGCTCCAA 240
TGCAGAAAGC GTGGGAAAGA AAGACGTATT CCGGGGTTTG TGCATCACAG GCTTAGGCTC 300
TGAGGGGAGT GGAAGTACCA GGGCGGAGAG GAACCTTCAG CAAAGATCCC ACGTGGCAGA 360
GGCTGAGCTG GAGAGGGTGA CCTCAGCAGG GAAGTGAGGA GAGCACAGAG CAGCCAACCA 420
GTTCCTGGCA GCTTTGGGAC CGTGTCTTCT GGGGACTGTG GCCAGGTTCA GGCTCAGCCC 480
TCACCCTTGG TGGTGACTCC GAGGCCGGCA GAGCCCCAAG TCAGCCTGTC CTGGGCAGGC 540
ACAAGGGTCC CACAGCAGGG TCACCCGGAG TCCCCAAGCT GGGCACCCTA AGGGGTGTCA 600
CCAGAGGAAA CACTTGGGTC TGTGGCTGAG GCTGAGGACC TGGCTGGGCA GAGGCCCCCA 660
TGGCCTTCAT GCCTCTGAGA AAGGGTCAGA AAACTCCTGA TGATGGAGGT TAAACAGCCG 720
TGGTCCCTGG GGCATGGAGG CCTGAATGCC ACTGAGCCAA GTTATGTGGA AACAAGGAAG 780
GCAGCATCCA GCACCACTGC CCATGGGAGA CTGTGGGCGT GACCAGGTCC TGCAGGGTTG 840
CAGAGGATGC CCAGGGGACC GGCAGCCCGG GGCTTGCAGG AGGGACCCCA GGCCCACTGA 900
GCTGCAACTT ATCAATTAAA CCCAAGGATT CAGGCCACGT GGTCCCAGAT GTGAAGTCGA 960
GCCCCAAAGC CACTATCAGA CTTTGGGATC CCAGCCAGGT CACCGGCCTC CCTGCTCCCG 1020
GCTCCCTCCT GGTCCAACAT GGACTGGGGG TCTGAGGAGT CCACGAAGCT ATGTGCTCGC 1080
TGCTCAGACA CTCACCCCCA CACGTGCTGT CACTGGCGGC TGGGCTCATA ATTGGAAACA 1140
GACCCATGTG ACTCAGAGGA AGCCAGCACT GCCCCAGCTC ACGCAGGCCC TCCTCGGAGC 1200
TTTAACAAGG GGCTAGCTTC CTGTGAGCCC CACTGTGTCC CACTGACATG TCAGCCACAC 1260
CGCTGAGTTC ATCCAGCCAG GGTGTCTTGG AAGGTTCTGT TCCCACGCAC GTAGCCAACA 1320
GCACCAGGCT ACACACACAC GTGTGGACAC ACATACACAC ACACACATGT GCGCACACAC 1380
ATCCACACGC ACATGCACAC ACACGTGCAT GCACATACAC ACCCACACAC GTGCACACAC 1440
ACGCGTGTAC ACTCGTACAC GCACATGGAC ACACACACGT ACACACATAC ACATGCACAC 1500
ATCCGTGGAC ACACACACAC ACATGCACAC ATGCGCACAC ACACGCACAC GCACATCGAG 1560
CTCCCATCAG CCCCTCGCGG CCACCCAGGA CACAGGATCA CAGTGAGCTG CAGTGACCAC 1620
TCAGGGCTCC CAACGCCCGT TCCGGGGACC CTTGCTGGGG ACTCTGCTTT GGAAAATGCA 1680
ACAGAGAACA 1690
|
