Variant report

Variant	rs73365118
Chromosome Location	chr7:52907225-52907226
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11238232	0.81[ASN][1000 genomes]
rs11974654	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11974657	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11978145	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11979464	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17135356	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34800110	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59672182	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62444519	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62444552	0.81[ASN][1000 genomes]
rs6951259	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6974952	0.85[ASN][1000 genomes]
rs725867	0.85[ASN][1000 genomes]
rs73365115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7784341	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888026	chr7:52588348-53013671	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv888031	chr7:52797324-52944424	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:52906600-52907400	Enhancers	NH-A	brain
2	chr7:52907000-52907400	Active TSS	Muscle Satellite Cultured Cells	--
3	chr7:52907000-52907400	Flanking Active TSS	Colon Smooth Muscle	Colon
4	chr7:52907000-52907400	Active TSS	Right Atrium	heart
5	chr7:52907000-52907400	Flanking Active TSS	HUVEC	blood vessel
6	chr7:52907000-52907600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:52907000-52907600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:52907000-52907600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:52907000-52907600	Enhancers	Placenta Amnion	Placenta Amnion
10	chr7:52907200-52907400	Flanking Active TSS	Ovary	ovary

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