| Tag | Content |
|---|
EnhancerAtlas ID | HS076-28114 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:10567730-10568550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr19:10568107-10568120 | GGGGGGGGGGGGG | - | 6.03 | | ZNF740 | MA0753.2 | chr19:10568108-10568121 | GGGGGGGGGGGGG | - | 6.03 | | ZNF740 | MA0753.2 | chr19:10568109-10568122 | GGGGGGGGGGGGG | - | 6.03 | | ZNF740 | MA0753.2 | chr19:10568112-10568125 | GGGGGGGGGGCAG | - | 6.33 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGCGCGGTG GCGGGTGCCT GTAATCTCAG CTACTCGGGA GGCTGAGGTA GGAAAATCGC 60
TTGAACCCGG GAGGTGGAGG CTACAGTGAG CCAGAGATCG TGCCACTGCA CTCCAGCCTG 120
GGCGACAGAG CGAGACTCTG TCTCAAGAAA AAAAGTGTTC GGTGTTTCCA GTACTCCCAC 180
CAGTGAGGGT GTGTCTCTGA GTTCTGAGGA TCCACCCAAT GGGAGCATAA CATGTAAATG 240
ACCCGTATTA GGCCTTTTCA TTGACTAGCT AGCTCCAGGT CACAATGGGT GACCTTGGCT 300
CAGCTCTGGA AGCCCCTGAA AGCTCAGGAA AAGGGTTCCT GGGGCTGTCC CCCAGGCAGG 360
CTGGTGCCAA GGTGGGCGGG GGGGGGGGGG GGCAGGGACA TGGAGCCAGA GACCACCCTT 420
CCCTCTCTCT TCCCAGTGAT GCCACCCCCC ACACCAGCAC TCTTGGCCCC CATGCTGGGA 480
TCTTCCCCAC CCAGAAAGGT TCCCTGGGTG TTCGGGGTAG GCAGCGGCTC TCCCTGGCAT 540
CCCCACCTCG CTTTCTGACT TCCCACACCA CTCTCCATCC ATATCTGATG ATCAGACCGG 600
GGCCATCCCA GAGCCCTGGG CCCCCACTCC AGCCCACCAC CTCCTGGAAG ATTTCCCACA 660
TCCCCTCTGG TTTCCTGACT CTGAGTAGCC AGCGGCATCA CAGCTGAAAG GGTTCTGCCG 720
TTTCGGGTGA GCCTTCCCCG TACGTGGTAG TGGGCTGAAG AATAAGGGAG CCTCCAGGGG 780
TGGAAGGGTT GTTCACACTT GTTCCTGCTC CCCATCTTCT 820
|
