Variant report

Variant	rs73648460
Chromosome Location	chr9:85223376-85223377
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10122746	0.84[EUR][1000 genomes]
rs10512132	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10512133	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10867862	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11139640	0.96[EUR][1000 genomes]
rs11139646	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11139648	0.80[AFR][1000 genomes]
rs11139649	0.80[AFR][1000 genomes]
rs11139650	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11139652	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11139653	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11139654	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11139661	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11139665	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11139680	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11139682	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11139683	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1571905	0.80[ASN][1000 genomes]
rs17085592	0.93[EUR][1000 genomes]
rs17085704	0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2001818	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73648462	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73648463	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73650741	0.96[EUR][1000 genomes]
rs7853040	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7853471	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7875519	0.93[EUR][1000 genomes]
rs7875637	0.93[EUR][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	nsv831641	chr9:85145561-85309589	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85221200-85227000	Weak transcription	Fetal Stomach	stomach
2	chr9:85221800-85223400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr9:85223200-85223800	Enhancers	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links