Tag | Content |
---|
EnhancerAtlas ID | HS170-00537 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr10:134373620-134374600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr10:134373809-134373819 | GTCACGTGAT | - | 6.02 | Myog | MA0500.1 | chr10:134373713-134373724 | CTGCAGCTGTC | - | 6.62 | TFEB | MA0692.1 | chr10:134373809-134373819 | GTCACGTGAT | - | 6.02 | Tcf12 | MA0521.1 | chr10:134373713-134373724 | CTGCAGCTGTC | - | 6.14 | USF2 | MA0526.2 | chr10:134373805-134373821 | CTGGGTCACGTGATAA | + | 6.11 |
|
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_10679 | chr10:134373572-134374270 | CD19_Primary | SE_11174 | chr10:134372713-134374921 | CD20 | SE_54289 | chr10:134373098-134374415 | Spleen | SE_61574 | chr10:134349316-134386582 | Toledo | SE_62964 | chr10:134349568-134409019 | Tonsil |
|
| 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 |
GH10I132559 | chr10 | 134373305 | 134374504 |
|
Enhancer Sequence | GTGTAGACCT GCTTGTGGAG TTGCTGTGTG AACATGTGTC TCCAGCTCTC TTGGGTGTAG 60 ACCTGCTTGT GGAGTTGCTG TGTGAACCTG TGTCTGCAGC TGTCTCGGGT GTAGACCTGC 120 TTGTGGAATT GCTGGGTCAC GATGTGTCTT CAGCTCTCTT GGGTGTAGAC CTGCTTGTGG 180 AGTTGCTGGG TCACGTGATA ATTCTGACTT TTTAAGGAAC TGCCAGACTC TTTCCACAGC 240 AGCTGCAGCA TTTTTCGTTC TTGTGAGCAG TGTCTGAGGG CTGCAGACTT CCAACATCAC 300 AGAACAGTAC TCGTGATTGT CCATCTTTTT TACTGTAACC GTCCTGGTGG GTGTGCAGTG 360 GTATCTCCTG GTGGCTTTGA ATTGCATTTC CCTGATGAGT AATCATGTTG AGTGTCTTTC 420 GTGTGCTTAC TGGGTATTTG TAGATCTGCT TTGAAGCAAC GCTTATTCAA ATCCATGGCA 480 CATTTTAATT TTTTTTTTTA AGAGACAGAT TCTCGCTCTG TTGCTCAGGC CGGAGGGCAG 540 TGGTGCGATG ATAGCTCACT GCAGCCTCCT CTTGGGCTCA AGGTATCCTC CCACCTCCCA 600 AGCAGCAGTG TCTCACGTAG CTGGGACTAC AGGTGTGTGT CAGCATGCTT GGCTAATTTT 660 AAAAAGTTTT AGTTTGTAAA TACAGGGTCT TGCTATGCTG TAGTCTGGTA TCAAACTGTA 720 GGCCTCAAGC AGTCCTCCTG CCTTGGCCTC CCAAAATGCT GGGATTATAG GTGTGAACCA 780 CCATGCCCAG GCTTTTTTTT TTTTTAATTG TTGAGTTTAA AGAGATCTTT ACATATTCTG 840 GATGCTAGAC CCTTATTAGA TAGATATGTA ATTTACAAAT GTTTTCTCTT GTTCTGTGTG 900 TTGTCTTCGC TTTTTTGATA GTGTCGTTTG AAGCACTTTT TTTTTTTTTT TTTTTGAGAC 960 AGGGTCTTCC CCTGTTGCCC 980
|