| Tag | Content |
|---|
EnhancerAtlas ID | HS145-10833 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr18:21002760-21003420 |
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 | CAGGTCACAA ACACCCCTCC CCCCCCCAAT GCAGAAAGCA CATCAGAATG CCAAATGAGT 60
GAGAGGGACA GCTGCTTGCT CTAATTGCTT TTTCATTTTA CTTGAGTCAT TCATAAATGT 120
CAAAACCCTG TTTTTCATGA TAAATGACTT GAGACACCAC ACCTCAGAAG TGACTATGAC 180
CACAACCCAC CCATGTGTTG CGACACTACA GTTGAGAACT CTGGCCTAAA GGACAAGTCA 240
CTTGGGTGTG ACACATAAAG TCCTTCGGGA CTTGCACCCG CCCCTCTCCA CGGTCAGCTC 300
CTGTCTGTCT GCTATGTGCA GCCACATTCC AGCCACAGCA GATGGCCCAC AGCCTTGGGA 360
ACATGCCAGG CCATGTCATA CTTCTAGGAG TCTGGTTGTG CCATCCTCTT GCCCCATAAT 420
GTTCTTCCCA TCTCTTTGTC TGTAGTGAAC ACCTGCTCAG CCTATAACAC CCAGTTTGCA 480
CATATCCTGT GTGAAGTTTC ACTGACCCAG CCAAGCAGAA CACACCAAAT GTGGGTCCTG 540
CCTTCAAACA GTTTGGTCCA GTACAGTGAT TCTCAACCAG GCAATCTTCC CCTCCAGGGG 600
GCATTTGGCA GTGTCTAGAG AAATGTTTGG TTGTTACAAC CGGGGGAGAG GAGCGGAAGG 660
|
