Variant report

Variant	rs7044450
Chromosome Location	chr9:85869597-85869598
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs58814988	1.00[AMR][1000 genomes]
rs7046038	1.00[AMR][1000 genomes]
rs7851573	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85854800-85890400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr9:85855000-85881400	Weak transcription	Adipose Nuclei	Adipose
3	chr9:85856200-85910600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr9:85861400-85873000	Weak transcription	Psoas Muscle	Psoas
5	chr9:85861400-85873000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr9:85863000-85873000	Weak transcription	Fetal Heart	heart
7	chr9:85863200-85873200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr9:85866000-85873000	Weak transcription	Left Ventricle	heart
9	chr9:85866200-85873600	Weak transcription	Right Ventricle	heart
10	chr9:85866200-85913000	Weak transcription	Aorta	Aorta

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links