| Tag | Content |
|---|
EnhancerAtlas ID | HS098-30482 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:70823440-70824790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr2:70824222-70824240 | AACATGCCCAGGCATGTC | - | 9.39 | | TP53 | MA0106.3 | chr2:70824222-70824240 | AACATGCCCAGGCATGTC | + | 9.6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_56248 | chr2:70822694-70827782 | u87 | | SE_67782 | chr2:70822694-70827782 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 70823463 | 70823663 | | chr2 | 70823866 | 70823963 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I070595 | chr2 | 70822998 | 70825124 |
|
Enhancer Sequence | TCTTTCTCCT TCCAGCCGCT GCTCAAATCC TACCCTCTTC CACCACCTCT TAAATCTTTT 60
TCCTGCCTGC ATTTTCTTAC ATAAAGCAAT CTACTACTGC CATCGGTTCA TTCACTCACC 120
GGAACCTGTC TTGCCAGGAC CTGACCTCAG CAGACTGAGT CATACCAGCA TCATCCTTGT 180
TGGGGCCCAG GTCTGCATCC CGCTTCCGGC CCCAGCCCCA CTGTTAGCTC CATCAGGTCC 240
TCTGGGGCAC ACCAAGGAGG CCGTTTTCTC TCCCTTTTTC TGAATTAGAT CCCCAGAAAC 300
AAGACATCAG GCTTCCTGGG GAAATCTAAT TTTGCTCATG AATTTGACCA TTCATTGTTG 360
CTCAGTTACC TGTGCCCAGC TCTTTCTGCC TTTTCAAACT GCACTCAGCT GTGCCCTTGA 420
ATGAACTGGG GCAGAAGTCC TTAGGTCCTG ATCACACATG CTGTTCCCAA CTTCCCTTCC 480
CCTTGACACG CTGTGGTGAA CTCTGAATTC CAGCACGTCT CCACTCTGCT GTAGAGCCTT 540
TCTAGGGCTG GCAAGCATTC TGCCACAGAG CTGGTCTTTG TGGCTTTATG CCCACAGTAA 600
TTACTAGGGC TGGGCCATGC AACCGTCTAA CCTCTTCAAT TTACAGCCTC CAGGATCTGC 660
CACCCCTGTG GCATTTGGAG GGTGTCTAAC CACAGACCGG ACGTGCGTGG TAGCAGGTGG 720
TCTGCTTGAT TGCTGGTCCT TCAGTGACCC CTCTGCTCTC CAGTGGCCAG ACAGGGATTC 780
AGAACATGCC CAGGCATGTC TGCTACTGAC GTCCTCATCC ATGAAATTCC CAATATCTGC 840
AGAAATTGTG TATTTGTACA TGTTGATTCT ATAATAAATA CTGAATCCCA GCCTGTACTG 900
CAGAAAGGCT TCCTTAGCCT CTCAGTCTGG CTTACGTAAA GCAGCGTAAG TGTGATTCTC 960
CATTTCACAC ACCGGGGCCC TTAACATTCC ATGCCCTCAT GGCTCTAATT CTGATTTTGG 1020
AACAGACCCC ACCATTTCCC TCTTTTTGAA GGTGACTTTG CAAGGATCAC ATAACTCCTG 1080
TTGGGCCAAC TTCCTTTCCC TTGTACTATG AGCATAACAA CTAGATGGTC AACCCGAAAG 1140
CTCATTCTTG TCACAGTTCT GGGGGGATCA GTTACCTGAA GCATACTCAG GTTGAAACCC 1200
CAGACAAACC TTACCAAATA TGATGTGAAC ATTCCAGTCT GCCCTGTAGA CCCTCACTAT 1260
GGTATCACAT CCCAATAAAC ACAAGCCCAC CTCAAAAGAA AAAAGAAAGA TTGATAAGTA 1320
ATGCAGGTCT TTACTTCTTG TAAACCCAGA 1350
|
