| Tag | Content |
|---|
EnhancerAtlas ID | HS105-74586 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:99160120-99161480 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr7:99160950-99160962 | TTTATTTTTAGA | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr7:99161159-99161174 | CGAACTCTTGACCTC | - | 6.24 | | STAT1 | MA0137.3 | chr7:99160533-99160544 | TTTCTAGGAAA | + | 6.14 | | Znf423 | MA0116.1 | chr7:99160441-99160456 | AGACCCCAGGGTGGC | + | 6.21 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27485 | chr7:99155363-99161884 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGACTTCCT TATTATTCGG TTTATCTATT TGAATTTCTT TACTTTCTTG TTTCTTCCTA 60
AGTATAAGGT CTCTGAGAAG GTCTGTAGAG TGTGGCTTAG ATTCCAGGAC TTAGAACCTC 120
TGAATCCTTA TCTTTCACAT CGTCTTCTCC GGGAGGGGTA ATTAACGTTT GTTTGGGGGT 180
GCCAAGAAGA GACATTCTCC TCCTTATCCC CAGTTCATGT TTATGGCCAT TGTGGGGCAT 240
CTTTTCCCTT TTAGCAAAGG GAAACTTTCT TGTGCTTTGC TTGATTTCTC ACCGTTCTTT 300
TCTTTTCCAT TTTTGTAGGA GAGACCCCAG GGTGGCCTCC CAACCTCCAA CCAGACACTT 360
TCCTCTTTGT TATCTCAGTG TCCCTGTATT AGAGAATTGA AGAATTTCCC ATTTTTCTAG 420
GAAAAAGAAA TGCCGTTTAT TTAAAAAGAC AGGCTAAATT CCTTCTTGTT GAGTAGTCCC 480
TCACCCCTTA AGATCCCCAG ATGTATCTCC AAGCAGGCAG AACTTGAGAT GTCATTTGAA 540
GGCATGACTC ACTGTGAGTA CATTTCAGTG AGTCACCCAG AATGGTAATC CCACGTAACC 600
ACACCCAGGG CAGCAGAAAT CTCAGATGTT TACCCCATGC TGAGGTGGGG TCAATGCTTA 660
ACTCATGTCT CTCCCTTGTC ATTTTGAAAG GTACAGTGGG AAGCTGGGAT TAGCCAAGCT 720
GTAGTGCTGC TGGGAAGCAT CAGTGGGGTT TGTCGGCAGC TCCCTTGGTG TGAGCATTGT 780
TCCTTTTTCT TTAGTTTATT TTTTATATTA TATTATATTT TTTATTTTAT TTTATTTTTA 840
GATGGAGTTT CACTCTTGTT GCCCAGGCTG GAGTGCAGTG GTGCAATCTC AACTCACTAC 900
AACCTCTGCC TTCCAGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGATT 960
ACAGGCATGG GCCACCACGC CCGCCTAATT TTGTATTTTT AGTAGAGACG GGGTTTCACC 1020
ATGCTGGTCA GGCTGATCTC GAACTCTTGA CCTCAAGTGA TCCACCTTCC TTGGCCTCCC 1080
AAAGTGCTGG AATTACAGGC ATGAGCCACC GCACCCAGCC TCCTTTTTCT TTAGTTTCTT 1140
GCTTGCTTCT GCACTCTTCT TTTTGTGTGT GTAAATACTG AATCATGCAT TTTCTTTTCT 1200
TTTTTTTTTT TCCGTTGGCT TTGTCTATGC TGGTGGCATC CAGGGCATTG CTTTGTCTCC 1260
CTGATTATGC TCAGGATTCA AGGTCTTCTT ATTTGTGGGG AGGCAGGCTG CCCACTGGGA 1320
CGGTTTTTAG TGTGTTTTCC ATTCCTGGCT CTTTAATCTT 1360
|
