| Tag | Content |
|---|
EnhancerAtlas ID | HS105-74719 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:100802840-100803790 |
Target genes | | Number: 27 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr7:100803086-100803097 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr7:100803086-100803097 | GATGAGTCACC | - | 6.62 | | PLAG1 | MA0163.1 | chr7:100803442-100803456 | CCCCCCAGGGCCCC | - | 7.03 | | ZNF263 | MA0528.1 | chr7:100803137-100803158 | TGAGGAGGGGGAGAGATGGGG | + | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34567 | chr7:100802020-100808455 | HCT-116 | | SE_65756 | chr7:100801977-100804101 | Pancreatic_islets |
|
| | 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 |
| GH07I101159 | chr7 | 100802601 | 100808148 |
|
Enhancer Sequence | CACCTGGTAG GTCATTCTTT TCTTCCCTGA TTTCTTCCCC CACCTCTCTT TTTTTTTTCT 60
TTTTTTTTTT TTTAACACAC ACATACTCCA AAGCCTCTGC GTCTCAGGAG GAAAAGGCTA 120
TGGGGATTTG GGGGCTGGCA GAGGGCACCT GGATGTTGGT TCTCCCTGCT CCCCAGCGCC 180
CCCGCCCTCA CCCCATTACT GCCTGCCCCC TCTCTGCTGT GCCATCACCG AGCCCTGGTG 240
CAGGGAGATG AGTCACCGGA ATCTGCAGTG ATGAGCGAGC CCGGCCTGAG CTGGCTCTGA 300
GGAGGGGGAG AGATGGGGGG CGAGGGAGGG CTCATCTTTG CAGTGGGAGA GAGGGCAGAA 360
CTGAACTTGC CACCTCACTG GTCGAGCTTC ACCTTCCCAC ACACGCACAC ACACACACCC 420
TGGCGCGCAC ACACACACAC ACACACACAT GCCCTGGCAC ACACACCCAT CGTGTCACCA 480
GTGTTGCGCT CAGACCCTAA TGACGCATCT CCCTGCAGCC TGGTTCACCT TCCCTCAGGG 540
ACCTGGCACT CACCTCCCTC TGCCTTTTCC CCACTCTGAA AAACAGGACC CAGTCAGCTG 600
TACCCCCCAG GGCCCCAGAA AGATCCCCCA CCTCCTTGTC CCGGCTTCAC TCCCTTTACC 660
CCCAGGTGTC AAGGCGGGGC CCCTGCTTAC CAAGGTCCTG GCTTTGGGTT CTCTGGGTGG 720
TGACGGACTC AACCTGGACC CCCCCTGCCA CTGTTGGCTG GCTCTGGGGC TGGCCCTGGG 780
AGGCTGGTGG GTGCCCCATG AAGGGCTCAC TGGTCCGGCC TTGGGCTCAC ATTGGCTTCT 840
CTCCCCCTCC CCCGTGTCTG TGCCTCCCCC GTCTGACTCT TCCTCGTGAC TGCTGTCTTG 900
CCCACCCTGT CGGCCTCTCC TGGTGTCTCT GCGTCACCCT CTGTCTGTCT 950
|
