| Tag | Content |
|---|
EnhancerAtlas ID | HS145-05422 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr12:23625120-23626040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr12:23625866-23625877 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr12:23625866-23625877 | CTGAGTCACCC | - | 6.02 |
|
| | 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 |
| GH12I023472 | chr12 | 23625361 | 23625510 |
|
Enhancer Sequence | TTTTTAATCC AGATGCATGC AAAGTCAGCC ATTCTTTGAC AACTTGGCAG CGTGGCTGTG 60
CAGGTATTTT AGCGTTGGGC CAGACACTGG AACACCTGTT CTGGGGTAGG GTAGGAACCT 120
TCACAGCCAG AACTGTAAAA AGCACCTCAG CAGTCACTGC TGAATTGCAG TCTTTCCTGT 180
CACAAGCCTG GGGTGGCAGT AGAGCTGCTA CAGCTGAAGT TTCTGCTGGG TGGAGAGACT 240
TGCAGCCAGG GCCAGCTGAA CAACATGGAA CTAATCTGCA TGTGCCACAA CTAGGTGCCC 300
TCCCCTGCCC CGCCCTGATA TTGTGGTGCA GCTAGGCCCA CTTCACTCCA GCCCCAGGCA 360
GAAATCTAGG TATTTGAATT ACCTGCTTGC CTGGACAGCA GCCTCAGCTG CCCCACCCTT 420
CCTGGACATA GATCATGATG AAGGGGGATT GGGGTGCCTC CGCTCCACAC CCAGGAAGAT 480
CTCCAGGTAA TTAGAGCACT TGAGCACCTG GATCAGCAAC CTGATTCATC TCACCCTTCC 540
TGTGCAGAGA TCCTGGTGCA GGGAGGCCTT TTCTGCTTCA CGCCCAGGCA AATCTCCAGG 600
CATTCGGAGC ACCTACTCGT CTGCTTCAAG AGCCTGAGTC ACTCCACCAC TCCTGGACAT 660
AGATTGTGGT GTAGGGGAGC CCTTTTTCCT CCACACCCAG GCAGATCTCC AGGCATTCAG 720
AGCACCAGAT CACCTGGATC AACAGCCTGA GTCACCCCAC CCTCTTATGC AGAGCTCCTG 780
GTGTAGGGCA GCCCTCTCTG CTCCATGCCC AGGCAGATCT CCAGCTATCT GGAGCACCCA 840
CTCTCTTGGA TTAGGAGTTT ACGACAGAGA ACAGACAGCA GCCCCTTTAC AGAGAACTTG 900
GGGATGAGGA GGTTTCCCAT 920
|
