| Tag | Content |
|---|
EnhancerAtlas ID | HS130-25154 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr7:100802870-100803790 |
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 | TTTCTTCCCC CACCTCTCTT TTTTTTTTCT TTTTTTTTTT TTTAACACAC ACATACTCCA 60
AAGCCTCTGC GTCTCAGGAG GAAAAGGCTA TGGGGATTTG GGGGCTGGCA GAGGGCACCT 120
GGATGTTGGT TCTCCCTGCT CCCCAGCGCC CCCGCCCTCA CCCCATTACT GCCTGCCCCC 180
TCTCTGCTGT GCCATCACCG AGCCCTGGTG CAGGGAGATG AGTCACCGGA ATCTGCAGTG 240
ATGAGCGAGC CCGGCCTGAG CTGGCTCTGA GGAGGGGGAG AGATGGGGGG CGAGGGAGGG 300
CTCATCTTTG CAGTGGGAGA GAGGGCAGAA CTGAACTTGC CACCTCACTG GTCGAGCTTC 360
ACCTTCCCAC ACACGCACAC ACACACACCC TGGCGCGCAC ACACACACAC ACACACACAT 420
GCCCTGGCAC ACACACCCAT CGTGTCACCA GTGTTGCGCT CAGACCCTAA TGACGCATCT 480
CCCTGCAGCC TGGTTCACCT TCCCTCAGGG ACCTGGCACT CACCTCCCTC TGCCTTTTCC 540
CCACTCTGAA AAACAGGACC CAGTCAGCTG TACCCCCCAG GGCCCCAGAA AGATCCCCCA 600
CCTCCTTGTC CCGGCTTCAC TCCCTTTACC CCCAGGTGTC AAGGCGGGGC CCCTGCTTAC 660
CAAGGTCCTG GCTTTGGGTT CTCTGGGTGG TGACGGACTC AACCTGGACC CCCCCTGCCA 720
CTGTTGGCTG GCTCTGGGGC TGGCCCTGGG AGGCTGGTGG GTGCCCCATG AAGGGCTCAC 780
TGGTCCGGCC TTGGGCTCAC ATTGGCTTCT CTCCCCCTCC CCCGTGTCTG TGCCTCCCCC 840
GTCTGACTCT TCCTCGTGAC TGCTGTCTTG CCCACCCTGT CGGCCTCTCC TGGTGTCTCT 900
GCGTCACCCT CTGTCTGTCT 920
|
