| Tag | Content |
|---|
EnhancerAtlas ID | HS139-55000 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:145100590-145101520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr8:145101176-145101190 | AGCCACGCCCCCTG | + | 6.17 | | KLF16 | MA0741.1 | chr8:145101177-145101188 | GCCACGCCCCC | + | 6.62 | | Myod1 | MA0499.1 | chr8:145100613-145100626 | AGGGGCAGCTGCA | - | 6.22 | | SP1 | MA0079.4 | chr8:145101174-145101189 | CTAGCCACGCCCCCT | + | 7.66 | | SP3 | MA0746.2 | chr8:145101176-145101189 | AGCCACGCCCCCT | + | 6.46 | | SP4 | MA0685.1 | chr8:145101174-145101191 | CTAGCCACGCCCCCTGC | + | 7.48 | | SP8 | MA0747.1 | chr8:145101177-145101189 | GCCACGCCCCCT | + | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34599 | chr8:145100141-145100887 | HCT-116 |
|
| | 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 |
| GH08I144045 | chr8 | 145100142 | 145100887 |
|
Enhancer Sequence | CGGGCAGGGC CAAGCCTGGA GGCAGGGGCA GCTGCACCTG TGACAGGCTG CAAGACTGGC 60
AGGGCCCAGT GCAAAATGAA AATAATTCAA AACTTAGAAC TTCAGGATGG TGCCAACAGC 120
GCATTGAGCT GGGCACTGGG CTTCCCACAA CTGCCCAGGT CACACATCCA GGGGGCAGCG 180
GCAGGCTGAG TGGGAGGGGC TGCCTTCATG ATTACATGCC TTAGGGCGGG AGCCAGTCAC 240
TGCCTGGCTG GTGGGAGGAC ACAGGGCATG AGGAAGTGAG TGGAAACTGA CCCAGATGTG 300
CTGGTTCCCA GGCCCTGGCC CTGGCCCCAG GCCCAGGAGG ACGCAGATGG AGACAGGCCC 360
CTCAGCGCTG GGGCCAACAC TTGCCTGGGG TTGTCAGTTC AGTGATGGGG GAGGAAAGGG 420
AGTCCCCTAG GGGGTGTGCA GGCTAGAGGG TGCTGAGGAT GGAGGCCAGG GTAAGGAAGG 480
GGGTGGCCTT CAGACGCTGA AAGGGAGCAG AGCACGGAGC CAGGAGGAGG CCTGGGAAAG 540
ACCCCAGACT CCTGGGTCAG GGGACCCTGT GCACCTCCAG ATGCCTAGCC ACGCCCCCTG 600
CCCTCAGTCC CTGGAGGCCT CAGCCCAGTT GCACTCCCTG GTGGTGCGTG GAGCAGACGA 660
CAGGGTTGGG GCATCCTCTT CCACCCTGTG GCTGAGGCCC TACTGGGGAG CTTTGAGAGC 720
CACCTGCCCT GCCCGGATCA GGCCTTGGAG ACCTGTCAGG CTCTGCCCAC TGGGTTCCCC 780
TGTCCTAGAT TCTTGAGGTC TGTCGCAGAA CCTCCCCACC GCACACCCCT CGGATCCTGG 840
CCATCTCACA GCCTCACCTG CCCCTCGGTC TTCCCCTTAC CTGCCTGTGT GTGGAGGTGT 900
GGCAAGGGAG GGTCCCTGAT GGCCGCTGTC 930
|
