| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23535 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:17400270-17401420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:17400791-17400806 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH19I017289 | chr19 | 17400200 | 17400809 |
|
Enhancer Sequence | TAAATAACCC GACTTCCAGC GATGCTATGC GACTTCAGAC CATTCATGTG CAAAGGTCTT 60
AAGTAAATAC CAAGCCGCCA TCCTGGTGAG ATGTCAGCGG TCTGGTTTCG GGCGGGCGGG 120
GGTCGGGGGG GGGTCGAGGG CATTTAAGCT TCTGGAAGTC GCTTCTGCAA AGGGCCCGGT 180
GCATTTAGGG ACTTGGGAGA GATCCGCTGC CTCATTGGTT TCAGGACCTG CCGGTCATCA 240
CGGCGGTTTA GCCAACCAGG TCCCCCAGGG GGCGGGCTGT GACCTGGGCC GAGTTTCCAC 300
CCACCTCGCC ACTGCTTAGC CACCGGCTGC TCCTCGGGGA ATGGCTGGTA TTGTGATTAG 360
GGGTCCAGTC TCTGGAGTGG GTTTGGGCTC GACCACTTGT AATCGAGCTG AAGAAACCGC 420
TCTCTGAGCT TCACTTTCCT CCAGTGTAAA ACAGGGGCCA GGCACCGTGG CTCACGCCTG 480
TACTCCCAGA ACTTTGGGAG GCCGAAGCGA GTGGATCACC TGAGGTCAGG AGTTCAAGAT 540
CAGCCTGGCC AACACAGTGA AACACTGTCT CTACTAAAAA TACAAAAATT AGCCGGGCGC 600
GGTGGCGGGT GTCTGTAATC TCAGCTACTC GGGAGGCTGA GGCAGGAGAA TCGCTTGAAC 660
CCAGGAGGCT GAGGCTGCAG TGAACCGAGA TTGTGCCACT GCACTCCAGC CTGGGTAACA 720
GAGCAAGACA CTGTCTCAGA AAAAAAAAAA AAAGTGTGAA ACAGGGATGC CTCCCAGTTG 780
CCAAATCTAA TAATAAAGCC ACAGGTGTTA TGACACTGTG CCATCGCCCC AGAATACACA 840
AACAGGACAT TGGTAAAGAA CCTAGAGCCC CCAGAAGAGA TGGGATTTGT CTAACACAGG 900
GTTTCCCAAT CTTGGCCCTA ATGACATTTG GGGTTGGCTT ATTCTTTGCT GTGGGGTCTG 960
TCCCTTGCAT TTCAGGGTGA TGAGCAGCGT TCCTGGCCTC CATCCACTAG AAGTCAGCAA 1020
CACCCATGCA CCCCCAAACA TGGCGATCAA AAATGTCTCC AGAAGTTGCC AATGGACACA 1080
ATTGCCCCCC TGGCTAAACT AAGGATGGAG CTCACAAACC GGTGGGGAAA GGACAGAACC 1140
GAGGGAAAGA 1150
|
