| Tag | Content |
|---|
EnhancerAtlas ID | HS051-14301 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:41955000-41955690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:41955429-41955448 | TCTCCACCAGGTGGCGCCA | + | 7.81 | | ZNF263 | MA0528.1 | chr19:41955049-41955070 | TCCCCTCCCCTCGCCTCCCCT | - | 6.04 | | ZNF263 | MA0528.1 | chr19:41955039-41955060 | CCTTTTCCCCTCCCCTCCCCT | - | 6.08 | | ZNF263 | MA0528.1 | chr19:41955034-41955055 | TTCCCCCTTTTCCCCTCCCCT | - | 6.14 | | ZNF263 | MA0528.1 | chr19:41955046-41955067 | CCCTCCCCTCCCCTCGCCTCC | - | 6.48 |
|
| | 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 |
| GH19I041449 | chr19 | 41954906 | 41955705 |
|
Enhancer Sequence | TCAGGAGAAG ATGGATGTCT CAGCTCCAAA CAAATTCCCC CTTTTCCCCT CCCCTCCCCT 60
CGCCTCCCCT CTTCTTTTTT TTTTTTTGAG ACAGAGTCTC GCTCTATCGC CCAGCCTGGA 120
GTGCAGTGGC GCGATCTCGG CAACCCCTCC GGGGTTGAAG CGATTCTCGT GTCTCAGCCT 180
CTCGAGTAGC TGGGATTACA GGAGCGCGCC ACATGTCCAG CTAATTTTTC TGTATTTTTT 240
AGTAGAGGGG ATGTTTCACC ATGTTGGCCA GGCTGGTCTC AAACTCCCGT CCTCATGTGA 300
TCCACCCACC TCGGCCTCCC AAAGTGCTGG AATTACAGGC GTGAGCCACA GCGCTTAGCC 360
AGAAAATTTT AAACATTACC CATGTTTTGG TTGTGCTTCT ACTGGGCTCC CACCTGCTGT 420
GATGCCCTGT CTCCACCAGG TGGCGCCAAC ACACCCCTGC AGCCCCTCCA GCCAAGGCAG 480
ACTGGACACT GAGGGGCAGG ACCCGACTAT GAGGTCCTTT GAGGAAGCAG GTCCTTATAG 540
AGGGCGTCGT TGAGACAGGC TATTCCCACA CAGGGGGCTC CTGTTGAGAG AGAAAGTCCA 600
AGTTCTGGTG AGCGGGAGAC AGGCAGGAAT AATCACTCCT AAAGCTACCC ATGTCACAAT 660
CCCTGGAACC CGTGAATGGT AACTTTTATG 690
|
