| Tag | Content |
|---|
EnhancerAtlas ID | HS017-24659 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr4:6695800-6696950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:6696285-6696303 | GGAAGGACGGGAGGAGGC | + | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr4:6696523-6696541 | TCTTCCTTCCTTCCCCTC | - | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr4:6696281-6696299 | GGCAGGAAGGACGGGAGG | + | 6.51 | | EWSR1-FLI1 | MA0149.1 | chr4:6696519-6696537 | ACTTTCTTCCTTCCTTCC | - | 8.12 | | KLF4 | MA0039.3 | chr4:6696003-6696014 | AGAGGGTGTGG | - | 6.02 | | ZNF263 | MA0528.1 | chr4:6696524-6696545 | CTTCCTTCCTTCCCCTCCCCT | - | 6.34 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32360 | chr4:6693831-6699251 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 6696206 | 6696267 | | chr4 | 6696335 | 6696668 |
|
Enhancer Sequence | AGCCAGGCCG GCAGTGCTGG ACTCAGCGGG GGCTGGGGAA GAAGGGGAAG GCGTGGCAGG 60
CAGAGGGCTG AGAGCTGCGG TGGGGTCGGC GGTCAAGGGG CTCAGAGGCA AGAGGGACAG 120
ATCCTGAAAT GCCCTGGAAG CCCAGCCAAG GAACGGACCC ACCCTGGCAT AAAGGCAGGG 180
GAGGCGGGAG CATCTGAGCA GGGAGAGGGT GTGGTCAGCT TGATCCTTGA AACATGGGGT 240
TGACCCCAGT GTATTTGTGA CAGGCCTGGT GGGAGAGTGG GACTCAAACC TGTGCAGTGG 300
GGGCAGGGGC GGAATGCAAT CCAGGGCTGC CATTTGCAAG TTTGCCAAGC TTGCCAAGCC 360
CTTGAGCCCT CGGGGCTGTC CTCCAAGGCT GCCGGCCATA AACGCCCCAG CTCTGCCTCC 420
CACTTGCCCG CTTTCCCTGC TCCCATTCCC AGGCCCCTTG TTGCCTGGTA TTAGTGGGTC 480
TGGCAGGAAG GACGGGAGGA GGCTCCATCC TGGCACCTGT CTGCGCAGAG CTGTGGACCT 540
CCCTTGGGCT CCCTGCCAGG GAGGAGCCAC CGGCCTGAGC CTCACAGAAG GCCCCTCAGG 600
GCGGCCAGGA CCAGCTTCCT TCCGCCCGGG GCAGCCTCCG GCTGGGCTGA ACAGAAGCCG 660
TACCCTCTCC ATTTCCCCTT CCCTTTGACC CCTGTCCTCT CCTTCTTTCT CACTCCCCCA 720
CTTTCTTCCT TCCTTCCCCT CCCCTTCGGG CCCCACCAGA CTCTGCCTAC CTGCTAAGGG 780
GCTAACCCAC ATAGATGCTG ATAATCAAAA ATGAAAGCCT GAAATTTTCA GCCCTAGAAT 840
CACTTCAAAG ACATGAAACA CTTCAGAATA TTGCTTCTAT TTTCTTTTCT TTTCTTTTTT 900
TTTTTTTTTG AGACAAGATG TCACTCTGTC ACCCAGGCTG GAGTGCAGTG GCAGGATCAC 960
GGCTCACTGC AGCCTCGACC TCCCTGGGCT CAGGTGATCC TCCCACCTCA GCCTACCGAG 1020
TAGCTGGGAC TACAGGTGCA TGTCACCATA CCCGGTTAAT TTTTGTATTT TTTTTAGAGA 1080
CAAGGTCTCA CCATGTTGCC CAGGCTGGTC TCAAACTCCT GTGCTCAGGC AATGCGTCAG 1140
CCTCGACATC 1150
|
