| Tag | Content |
|---|
EnhancerAtlas ID | HS136-20627 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr9:134231130-134232220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr9:134231286-134231298 | AAACAAACAAAC | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr9:134231369-134231384 | 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 |
| GH09I131356 | chr9 | 134231987 | 134232188 |
|
Enhancer Sequence | AATAGCCTGG CCAACATGGT GACACCCCAT CTCTACTAAA AATACAGAAA TTACCTGTAG 60
TCCCAGCTAC CTGGGAGGCT GAGGCAGGAG AATCACTTGA ACCTGGGAGG CGGAGGTTGC 120
AGCGAGCCAA GATCGTGCCA TTGCACTCCG TCTCAAAAAC AAACAAACAA AACCAGGCTG 180
GGGGTGGTGG CTCATGCCTG TTATCCCAGA ACTTTGGGAG GCTGAGACAG GTGGATCACG 240
AGGTCAGGAG TTCAAGATCA ACCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA 300
CAAAAATTAG CTGGGCGTGG TGGTGGGCGC CTGTAATCCC AGCTACTCGG GAGGCTGAGG 360
CAGGAGAATT GCTTGAACTT GGGAGGCAGA GGCTGCAGTG AGCGAAGATC GCGCCACTGC 420
ACTCCAGCCT GGATGACTCC ATCTCAAAAA AAAAGGCCAA GTGTGGTGGC TCACACCTGT 480
AATCCCGGCA CTTTGGGAGG CCGAGGTGGG TGGATCACCT GAAGTCAGGA GTTTGAGACC 540
AGCCTGACCA ACATAGTGAA ACCTCATCTC TACTAAAAAT ACAAAATTAG CTGGGTGTGG 600
TGGCACATGC CTGTAGTTCC AGCTACTTGG GAGGCTGAGG CAGGAGAATG ACTTGAACCT 660
GGGAGGTGGA AGTTGCAGTG AGCAAAAGTC ACACCATTGC ACTCCAGCCT GGGCAATAAG 720
AGAGAAACTC CATCTCAAAA AAAAAAAAAA AAAAAAAAAA GAAGAGCTCA TGTCATCCGC 780
AAATAGAGAC AGTTTTACTT CCTTCCCAAT GTGGATGCCT TTTACTTCCC TTTCTTGCCT 840
AATTGTTCTG GCGAGAACGT CCAGTGCACT GCTGATAGAA GTGACCAGAG CAGGCATCCT 900
TGGGTTGTTT CTGCAGAGGC TGAACTTTTA ACCGCATGAT GGACTTTTTC TGCTGAGTCG 960
TCCTGATTCT TGGTTTGTGG GGAAAAGCAA GAGAGATCAG ATTGTTACTG TGTCTGTGTA 1020
GAAAGAAGTA GACATAGGAG ACTCCATTTT GTTATGTACT AAGAAAAATT CTTCTGCCTT 1080
GAGATTCTGT 1090
|
