Variant report

Variant	rs475164
Chromosome Location	chr11:85010766-85010767
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:85010195..85012743-chr11:85014676..85016678,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10898380	0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap]
rs10898382	0.89[CHB][hapmap];0.95[JPT][hapmap]
rs11234316	0.84[CHB][hapmap];0.89[JPT][hapmap]
rs12419394	0.85[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1517311	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1682383	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810088	0.85[CHB][hapmap]
rs1793210	0.86[ASN][1000 genomes]
rs1826612	0.88[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs1914373	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1914376	0.89[ASN][1000 genomes]
rs2138748	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs286044	0.84[ASN][1000 genomes]
rs286499	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs286513	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs286515	0.88[CEU][hapmap];0.89[CHB][hapmap];0.89[JPT][hapmap]
rs2930575	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35167573	0.83[ASN][1000 genomes]
rs473968	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs474992	0.89[ASN][1000 genomes]
rs476781	0.94[ASN][1000 genomes]
rs488668	0.90[ASN][1000 genomes]
rs4943918	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs4944513	0.85[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs495905	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs496814	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs497607	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs500307	0.90[ASN][1000 genomes]
rs508177	0.91[ASN][1000 genomes]
rs512775	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512910	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs514639	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs516080	0.90[ASN][1000 genomes]
rs516620	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs519429	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs526990	0.85[ASN][1000 genomes]
rs527928	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs530293	0.94[ASN][1000 genomes]
rs531331	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs534604	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs539551	0.98[ASN][1000 genomes]
rs550981	1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs603170	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs680675	0.81[ASN][1000 genomes]
rs7106588	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7110363	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs7111281	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs789599	0.96[ASN][1000 genomes]
rs938728	0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs951729	0.84[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84967800-85019400	Weak transcription	Ovary	ovary
2	chr11:85009600-85011200	Enhancers	A549	lung
3	chr11:85010200-85010800	Enhancers	Fetal Intestine Large	intestine
4	chr11:85010400-85011200	Enhancers	Colon Smooth Muscle	Colon
5	chr11:85010600-85021600	Weak transcription	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links