Variant report

Variant	rs35089927
Chromosome Location	chr9:85099517-85099518
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:85092539..85095359-chr9:85099024..85100878,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1041392	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11139569	0.89[ASN][1000 genomes]
rs11139570	0.93[ASN][1000 genomes]
rs12350753	0.89[ASN][1000 genomes]
rs12553129	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12683121	0.92[ASN][1000 genomes]
rs12683715	0.92[ASN][1000 genomes]
rs12684844	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12685162	0.92[ASN][1000 genomes]
rs13298628	0.98[ASN][1000 genomes]
rs13299917	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1330817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1411660	0.92[ASN][1000 genomes]
rs1411661	0.85[ASN][1000 genomes]
rs1411662	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17085530	0.92[ASN][1000 genomes]
rs17085531	0.92[ASN][1000 genomes]
rs2026194	0.91[ASN][1000 genomes]
rs2889949	0.91[ASN][1000 genomes]
rs34637520	0.93[ASN][1000 genomes]
rs34845422	0.85[ASN][1000 genomes]
rs34867546	0.85[ASN][1000 genomes]
rs35501117	0.88[ASN][1000 genomes]
rs35576282	0.92[ASN][1000 genomes]
rs35677430	0.92[ASN][1000 genomes]
rs4478643	0.81[ASN][1000 genomes]
rs4877232	0.93[ASN][1000 genomes]
rs4877233	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4877692	0.93[ASN][1000 genomes]
rs4877693	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56291243	0.90[ASN][1000 genomes]
rs67968529	0.92[ASN][1000 genomes]
rs7018522	0.89[ASN][1000 genomes]
rs7021813	0.92[ASN][1000 genomes]
rs7036901	0.92[ASN][1000 genomes]
rs7037151	0.92[ASN][1000 genomes]
rs7046852	0.91[ASN][1000 genomes]
rs7850032	0.84[ASN][1000 genomes]
rs7850751	0.90[ASN][1000 genomes]
rs7865259	0.84[ASN][1000 genomes]
rs7865649	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][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	nsv893510	chr9:84954592-85117420	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85098200-85103000	Weak transcription	NHEK	skin
2	chr9:85098800-85099600	Enhancers	HepG2	liver

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