Tag | Content |
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EnhancerAtlas ID | HS065-04686 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr7:100802990-100803790 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34567 | chr7:100802020-100808455 | HCT-116 | SE_65756 | chr7:100801977-100804101 | Pancreatic_islets |
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| 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 |
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Enhancer Sequence | GGATGTTGGT TCTCCCTGCT CCCCAGCGCC CCCGCCCTCA CCCCATTACT GCCTGCCCCC 60 TCTCTGCTGT GCCATCACCG AGCCCTGGTG CAGGGAGATG AGTCACCGGA ATCTGCAGTG 120 ATGAGCGAGC CCGGCCTGAG CTGGCTCTGA GGAGGGGGAG AGATGGGGGG CGAGGGAGGG 180 CTCATCTTTG CAGTGGGAGA GAGGGCAGAA CTGAACTTGC CACCTCACTG GTCGAGCTTC 240 ACCTTCCCAC ACACGCACAC ACACACACCC TGGCGCGCAC ACACACACAC ACACACACAT 300 GCCCTGGCAC ACACACCCAT CGTGTCACCA GTGTTGCGCT CAGACCCTAA TGACGCATCT 360 CCCTGCAGCC TGGTTCACCT TCCCTCAGGG ACCTGGCACT CACCTCCCTC TGCCTTTTCC 420 CCACTCTGAA AAACAGGACC CAGTCAGCTG TACCCCCCAG GGCCCCAGAA AGATCCCCCA 480 CCTCCTTGTC CCGGCTTCAC TCCCTTTACC CCCAGGTGTC AAGGCGGGGC CCCTGCTTAC 540 CAAGGTCCTG GCTTTGGGTT CTCTGGGTGG TGACGGACTC AACCTGGACC CCCCCTGCCA 600 CTGTTGGCTG GCTCTGGGGC TGGCCCTGGG AGGCTGGTGG GTGCCCCATG AAGGGCTCAC 660 TGGTCCGGCC TTGGGCTCAC ATTGGCTTCT CTCCCCCTCC CCCGTGTCTG TGCCTCCCCC 720 GTCTGACTCT TCCTCGTGAC TGCTGTCTTG CCCACCCTGT CGGCCTCTCC TGGTGTCTCT 780 GCGTCACCCT CTGTCTGTCT 800
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