| Tag | Content |
|---|
EnhancerAtlas ID | HS091-32652 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:24108480-24109560 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr22:24108735-24108745 | TTCAAGTGGT | - | 6.02 | | ZNF263 | MA0528.1 | chr22:24108968-24108989 | GGTGCAGGAGAGGGAGGAGAA | + | 6.97 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGCTGCAGG ATCAGCTTGG AGTTGGCACC TGGAGGTGCG TTTCAAACCT GGGGCCACCT 60
GCCCCTCCCC ACATCCCCAG CCTGGGTGTC CCAAGGGTCC TAGGCAGGCT GAGTGATCCA 120
GCAGCAGAGG CGGCTACAGA CAGCATGTTT CTGCTGCCTT TTTTTTTTTT TTTTTTTGAG 180
ACAGAGTCTC ACTCTGTCAC CTAGAGTGGA GTGCAGCGGC GCAGTCTCGG CTCACTGCAA 240
CCTCCGCCTC CCGGGTTCAA GTGGTTGTCC TGCCTTGGCC TCCCAAGTAG CTGGGGCTAC 300
AGGCGCCCGC CACCATGCCC AACAAATTTT TTGTATTTTT AGTAGAGAGG GGGTTTCACT 360
ATGTTGGCCA GGCTGGTATC GAACTCCTGA ACTCATGATC CACCCGCCTT GGCCTCCCAA 420
AGTGCTGGGA TTACAGGCAT GAGCCACTGC GCCTGGCCTC TGCTGCCTTC TAATGGGCAC 480
TTTGGGCGGG TGCAGGAGAG GGAGGAGAAG GCTCTAGGAA AGCCCAGTAC TCTGCCTGTA 540
CTCTCAGAGT ATGAGCCCCA CCCCCACAAG TTCTAGCACC TTCCTGGCTC AGCTACACTA 600
ATCCTCATGA CCCCTGACCT AGCCACAAAG CCACATTTGG CTTACGGCGG TGGGGTTCCT 660
AGCAGGGGAA AGGTCATCAG GGAAGTGGCT CCCCTTCGCC CTTGCGCCCA GCGGCCACAG 720
TGCCCAGACC TGGGTGTGGG GAGAACAGGG GCTCAGGAAA TCCAACATCC CTCCCCTCTG 780
CTAGGGTGAG GTGACCTTGG GCGAGTCTCT GAGCCCTCAG GGCCTGGGTT TCCCATCTTT 840
AAAGGGCTGG TTGGTGTCTC TCCCTGGGAG CTTAGGGACC CTGGCCTCAA GGGAGAGGCC 900
GGGAAGCCTG CCTCTAAGTG ACAGTGAACT CAAGACCAGT GGACTAGGAC CCTTCCCGGG 960
CAGAGTCCTG GGCTGAAGCA ATGGTGAATA CACGCGGACA CTCCTCACTG GACACTTGGG 1020
CAGCTCCCTG TGTGGCCTCG AGATAATCCT GCCTCAGTTT CTCTTGGACT CGCTGCTCAC 1080
|
