Variant report

Variant	rs60163449
Chromosome Location	chr16:79925921-79925922
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:79924695..79926567-chr16:79927606..79930494,2	MCF-7	breast:
2	chr16:79918519..79921940-chr16:79923355..79927904,4	MCF-7	breast:
3	chr16:79919007..79921111-chr16:79925288..79927075,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10514468	0.91[EUR][1000 genomes]
rs12149386	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12149402	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12149430	0.91[EUR][1000 genomes]
rs4421996	0.91[EUR][1000 genomes]
rs4423433	0.91[EUR][1000 genomes]
rs4578665	0.91[EUR][1000 genomes]
rs55731323	0.82[ASN][1000 genomes]
rs56015959	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60450864	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7196167	0.82[ASN][1000 genomes]
rs7196727	0.82[ASN][1000 genomes]
rs7197500	0.82[ASN][1000 genomes]
rs7198100	0.82[ASN][1000 genomes]
rs7204861	0.82[ASN][1000 genomes]
rs73576036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73576037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73576054	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73576055	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73576058	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73576065	1.00[EUR][1000 genomes]
rs73576077	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74038077	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs74038078	0.91[EUR][1000 genomes]
rs74038079	0.91[EUR][1000 genomes]
rs74038082	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74038084	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74040120	0.93[ASN][1000 genomes]
rs74040137	0.91[EUR][1000 genomes]
rs74040138	0.91[EUR][1000 genomes]
rs74040147	0.91[EUR][1000 genomes]
rs8049733	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv573290	chr16:79853267-79939504	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv573291	chr16:79881386-79931595	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv906994	chr16:79883850-79928186	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv457555	chr16:79893737-79926134	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv471100	chr16:79893737-79926134	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv573292	chr16:79893737-79926134	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv457556	chr16:79896825-79926134	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv573293	chr16:79896825-79926134	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79908800-79931400	Weak transcription	Right Atrium	heart
2	chr16:79925800-79926800	Weak transcription	K562	blood
3	chr16:79925800-79929200	Weak transcription	Fetal Intestine Large	intestine

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