| Tag | Content |
|---|
EnhancerAtlas ID | HS105-36928 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr18:21002450-21003460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr18:21002823-21002836 | AGGGACAGCTGCT | - | 7.52 | | TCF3 | MA0522.2 | chr18:21003207-21003217 | AACACCTGCT | + | 6.02 | | TP53 | MA0106.3 | chr18:21003119-21003137 | AACATGCCAGGCCATGTC | + | 6.31 | | TP53 | MA0106.3 | chr18:21003119-21003137 | AACATGCCAGGCCATGTC | - | 6.77 |
|
| | 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 |
| GH18I023420 | chr18 | 21000838 | 21004105 |
|
Enhancer Sequence | TCTTCCCCAC CAACCCTCCT GCCTCTGTCT CAATTCAGGC TCTCATCATC TCATGCCTGG 60
CTCACAGCAT TAGTCCCTTA ACTGGTCCCC CTCTCTCCAA GGTTGCCCCC CATCCATTCT 120
TTACTTTGCA GTCAAAGCGT TTGTCCTAAA ATGCAAATTT AATTGAGCTA CTCGCTTGTT 180
TTAAAAACAG ATGATTCTTC CTGCTGCCAC AGGCAGCAAC CCTCAGCCTC TTTTCTGTCA 240
ACAACACATT CGGGGTCATG AAGCTCACCT GAGACACACA GCCCCCAGCA TGCACAGTGC 300
AGGGGCAGCA CAGGTCACAA ACACCCCTCC CCCCCCCAAT GCAGAAAGCA CATCAGAATG 360
CCAAATGAGT GAGAGGGACA GCTGCTTGCT CTAATTGCTT TTTCATTTTA CTTGAGTCAT 420
TCATAAATGT CAAAACCCTG TTTTTCATGA TAAATGACTT GAGACACCAC ACCTCAGAAG 480
TGACTATGAC CACAACCCAC CCATGTGTTG CGACACTACA GTTGAGAACT CTGGCCTAAA 540
GGACAAGTCA CTTGGGTGTG ACACATAAAG TCCTTCGGGA CTTGCACCCG CCCCTCTCCA 600
CGGTCAGCTC CTGTCTGTCT GCTATGTGCA GCCACATTCC AGCCACAGCA GATGGCCCAC 660
AGCCTTGGGA ACATGCCAGG CCATGTCATA CTTCTAGGAG TCTGGTTGTG CCATCCTCTT 720
GCCCCATAAT GTTCTTCCCA TCTCTTTGTC TGTAGTGAAC ACCTGCTCAG CCTATAACAC 780
CCAGTTTGCA CATATCCTGT GTGAAGTTTC ACTGACCCAG CCAAGCAGAA CACACCAAAT 840
GTGGGTCCTG CCTTCAAACA GTTTGGTCCA GTACAGTGAT TCTCAACCAG GCAATCTTCC 900
CCTCCAGGGG GCATTTGGCA GTGTCTAGAG AAATGTTTGG TTGTTACAAC CGGGGGAGAG 960
GAGCGGAAGG TATGCCACTG GAATCTAGCC AGTAGAAGCC AGGGATGCTG 1010
|
