| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38951 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:11137510-11138450 |
Target genes | | Number: 32 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:11138429-11138450 | GCCTTCTCTCCTGCCTCCTCC | - | 6.73 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTATTAACC CCAAGAGACA GGATTCCTGA GGCAGACCTG GCTTACAGAT CCCACTCTGC 60
CGCCTCCAAG CTCTGTGACT CTAGACAGCT TTCTTAACCT CTCTGAGCCT AAACTCTGCT 120
CACTAGTACA GAGGCACTCT TTACATCATG TGGGTGTTTT CTATAGCACC CTTTGTAAGG 180
GGCAGCCCAG ACTCCTTTAA GCCCCTAATG GATGTGGATG CTGTGTCTAG ATTTTCACCA 240
TTGCAAAGAA CCTTGCTAAA AGCATTCTTC CAGCTAAAGC CTCCATTCAA TTCCCCTGGG 300
GTAGTAAGCC ATTTGCAAGA AGAGAGGCGC CTAATGAAAA CATCACAAAT TCTTTTTGAT 360
GTGTTTTTTT ATACTGAGTT GTGGAACAGG GTCCTGTACA CCTGGCTTCA AGGCTGGGAG 420
GCCTGGCTTG GACATGTGGT CAGCCATATC ACGTCGTCCC CCTGCCAGCC TCAGTGTCCA 480
CATCTACAAC ACTTGGGGTT TGGCTGGAGA GAACATGAGA AGCCGAGGTG GCCCTTCCTT 540
CTGGGTCTAG CAGAGCATGG GTGTCTCCAG TGTGGCATTT GCTCCTGGGG CTTCTTTATC 600
GGGCAAGGGG ACAAGGTCTG GCTTCCCGGA GCATCCCTGT TCCAGCCCCG TGTTGTGCCG 660
GCCATGTGAC TCACAGCTCC TCTCATTTTC ATGAGTGTCT GGGTTTGACG AGAAATACAT 720
GTGCCACCCT GGTGATACGC CTCCCCAGCG AGGGTGGCCG GGCTTATTTC AGTTGGGGGA 780
AATGGCTTTG CTGAAGCTTT GGGTGGGTGA CGTCTGCTTA GGATGCATGT CTGTGCCCTT 840
GAACCCGGCG CCTGGCCTGG AGGCGGGCGA TGCACCTCCT GCCTTACCTG CCTGCAGGGT 900
TCCAGGTTTA ACATCCTGCG CCTTCTCTCC TGCCTCCTCC 940
|
