| Tag | Content |
|---|
EnhancerAtlas ID | HS002-03918 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr16:69757500-69758390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr16:69757704-69757716 | AAACAAACAAAC | - | 6.32 | | HNF4G | MA0484.1 | chr16:69757913-69757928 | AAGGGACAAAGTTCA | + | 6.5 | | Hnf4a | MA0114.3 | chr16:69757914-69757930 | AGGGACAAAGTTCAAC | + | 6.27 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35409 | chr16:69754257-69762210 | HepG2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 69757694 | 69758020 | | chr16 | 69758026 | 69758185 |
|
Enhancer Sequence | GACCAGCCTG GTTAACATGG TGAAACCCCG TCTCTACTAA AAATACAAAA AAAAATTAAC 60
CAGGTGTAGT GGCAGGTGCC TGTAATCCCA GCTAATCGGG AGGCTGAGGC AGGAGAATTG 120
CTTGAATCCA GGAGGCGGAG GTTGCAATGA GCCGAGATCG CACCATTGCA CTCCAGCCTG 180
CGCAACAGAG CAAGCCTCTG TCTCAAACAA ACAAACAAAA AGATGCTTGT GAATAGGCAA 240
TTTAAAAGTT TTCTGGGCCC TGGAGGGTTC ATTTTCCCTT CCTGCCACTT AACTAGCTGA 300
GCAACATGAC CTGGGAGGAG TTAGACTATT AGAGTTTACC CTGAGAGAGG CCACAAGATG 360
CACACACGGA TAACCTCTTC AGGGTACAAT GGCATTAGTG TGTTAGGAGA GGTAAGGGAC 420
AAAGTTCAAC AGAAGGCTGG GTGTGGTGGC TCATGCCTGT AATCGTAGCA CTTTGGGAGA 480
CCGAGGCGGG TGGATTACTT GAGGTCAGGA GCTAGAGACC AGCCTGGCCA ACATGGTGAA 540
ACCCCGTCTC TACTAAAAAT ACACAATTAG CTGGGCGTGG TGGTGGGCGC CTGTAATCCC 600
AGCTACTTGG GAGGCTGCAG CACAAGAATC GTTTGAACCT GGGAAGTGGA GATTGCAATG 660
AGCCAAGATC ACGCCACTGC ACTACAGCCT GGGCAACAGA GTGAGTGAGA CTCCATCTCA 720
AAAAGTTCAA CAGAGGAAAA CTTCAGGACC TCAGGGCTGG CCCATTCGGA AAGGCCCTCA 780
GAGGAGCTTG CCATTTGAGC TGAATCTTGG TCTTGAACTC CTGGCCTCAA GCAGTCCTCC 840
CGCCTCAGCC TCCCAAAAGT GCTGGGATTA CAGGAATGAG CCACCACTCC 890
|
