Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10493462	1.00[EUR][1000 genomes]
rs12079486	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12084223	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17131144	1.00[EUR][1000 genomes]
rs17131147	1.00[EUR][1000 genomes]
rs17131149	1.00[EUR][1000 genomes]
rs17131153	1.00[EUR][1000 genomes]
rs17131173	1.00[EUR][1000 genomes]
rs17131175	1.00[EUR][1000 genomes]
rs17131185	1.00[EUR][1000 genomes]
rs17131194	1.00[EUR][1000 genomes]
rs17131195	1.00[EUR][1000 genomes]
rs17131197	1.00[EUR][1000 genomes]
rs17131198	1.00[EUR][1000 genomes]
rs58361762	1.00[EUR][1000 genomes]
rs72915800	1.00[EUR][1000 genomes]
rs72917803	1.00[EUR][1000 genomes]
rs72917809	1.00[EUR][1000 genomes]
rs72926213	1.00[EUR][1000 genomes]
rs72943277	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72943286	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72945223	1.00[EUR][1000 genomes]
rs72945229	1.00[EUR][1000 genomes]
rs72945240	1.00[EUR][1000 genomes]
rs970938	1.00[EUR][1000 genomes]
rs970939	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428466	chr1:70306638-70455357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv525370	chr1:70361833-70367087	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70366600-70367600	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr1:70366600-70368000	Enhancers	Primary monocytes fromperipheralblood	blood

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