Variant report

Variant	rs166839
Chromosome Location	chr17:19789123-19789124
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs115326	0.87[EUR][1000 genomes]
rs118943	0.87[EUR][1000 genomes]
rs123081	0.88[EUR][1000 genomes]
rs123082	0.97[EUR][1000 genomes]
rs150122	1.00[EUR][1000 genomes]
rs157387	0.97[EUR][1000 genomes]
rs157388	1.00[EUR][1000 genomes]
rs157389	1.00[EUR][1000 genomes]
rs157390	1.00[EUR][1000 genomes]
rs157391	0.97[EUR][1000 genomes]
rs157392	0.97[EUR][1000 genomes]
rs157394	0.97[EUR][1000 genomes]
rs157395	1.00[EUR][1000 genomes]
rs157396	1.00[EUR][1000 genomes]
rs157397	0.97[EUR][1000 genomes]
rs157399	0.94[EUR][1000 genomes]
rs157400	1.00[EUR][1000 genomes]
rs157401	1.00[EUR][1000 genomes]
rs157402	1.00[EUR][1000 genomes]
rs157403	1.00[EUR][1000 genomes]
rs157406	0.97[EUR][1000 genomes]
rs157408	1.00[EUR][1000 genomes]
rs157409	1.00[EUR][1000 genomes]
rs166838	0.97[EUR][1000 genomes]
rs169460	0.91[EUR][1000 genomes]
rs169512	0.97[EUR][1000 genomes]
rs169513	0.97[EUR][1000 genomes]
rs172186	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs176098	1.00[EUR][1000 genomes]
rs182214	1.00[EUR][1000 genomes]
rs184006	1.00[EUR][1000 genomes]
rs188138	1.00[EUR][1000 genomes]
rs192511	0.97[EUR][1000 genomes]
rs205090	0.97[EUR][1000 genomes]
rs205093	0.87[EUR][1000 genomes]
rs205094	0.87[EUR][1000 genomes]
rs205096	0.87[EUR][1000 genomes]
rs205097	0.84[EUR][1000 genomes]
rs205098	0.87[EUR][1000 genomes]
rs205099	0.87[EUR][1000 genomes]
rs205100	0.87[EUR][1000 genomes]
rs205103	1.00[EUR][1000 genomes]
rs205104	1.00[EUR][1000 genomes]
rs205105	1.00[EUR][1000 genomes]
rs205106	0.97[EUR][1000 genomes]
rs205107	0.87[EUR][1000 genomes]
rs205108	0.84[EUR][1000 genomes]
rs205110	0.87[EUR][1000 genomes]
rs205111	0.84[EUR][1000 genomes]
rs205112	0.87[EUR][1000 genomes]
rs205113	0.87[EUR][1000 genomes]
rs2385963	1.00[EUR][1000 genomes]
rs281325	0.94[EUR][1000 genomes]
rs281326	1.00[EUR][1000 genomes]
rs281327	1.00[EUR][1000 genomes]
rs281328	0.97[EUR][1000 genomes]
rs281329	0.87[EUR][1000 genomes]
rs281331	0.97[EUR][1000 genomes]
rs281332	0.97[EUR][1000 genomes]
rs281333	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs281334	0.97[EUR][1000 genomes]
rs281336	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs281337	1.00[EUR][1000 genomes]
rs281338	0.97[EUR][1000 genomes]
rs281339	0.94[EUR][1000 genomes]
rs281341	1.00[EUR][1000 genomes]
rs281342	1.00[EUR][1000 genomes]
rs281343	1.00[EUR][1000 genomes]
rs281344	0.97[EUR][1000 genomes]
rs281345	0.97[EUR][1000 genomes]
rs281346	1.00[EUR][1000 genomes]
rs281347	0.94[EUR][1000 genomes]
rs281348	1.00[EUR][1000 genomes]
rs281349	0.97[EUR][1000 genomes]
rs281350	1.00[EUR][1000 genomes]
rs281351	1.00[EUR][1000 genomes]
rs281352	0.93[EUR][1000 genomes]
rs281353	0.97[EUR][1000 genomes]
rs281354	1.00[EUR][1000 genomes]
rs281355	1.00[EUR][1000 genomes]
rs281356	0.97[EUR][1000 genomes]
rs281365	1.00[EUR][1000 genomes]
rs3098902	0.97[EUR][1000 genomes]
rs3098905	1.00[EUR][1000 genomes]
rs3098906	0.97[EUR][1000 genomes]
rs3098907	1.00[EUR][1000 genomes]
rs3098908	0.97[EUR][1000 genomes]
rs3098909	0.97[EUR][1000 genomes]
rs3101810	0.97[EUR][1000 genomes]
rs3101811	1.00[EUR][1000 genomes]
rs3101812	1.00[EUR][1000 genomes]
rs3101813	1.00[EUR][1000 genomes]
rs3101814	0.97[EUR][1000 genomes]
rs3101815	1.00[EUR][1000 genomes]
rs34372768	1.00[EUR][1000 genomes]
rs367383	1.00[EUR][1000 genomes]
rs379703	1.00[EUR][1000 genomes]
rs383948	0.93[EUR][1000 genomes]
rs383951	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs394009	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs395130	0.97[EUR][1000 genomes]
rs421561	1.00[EUR][1000 genomes]
rs445958	0.94[EUR][1000 genomes]
rs4586510	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4924800	1.00[EUR][1000 genomes]
rs4925047	0.87[EUR][1000 genomes]
rs6587203	0.87[EUR][1000 genomes]
rs7225417	0.87[EUR][1000 genomes]
rs917519	0.87[EUR][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	nsv1062853	chr17:19547912-20206601	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv1063892	chr17:19564634-19808485	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv482398	chr17:19673458-19808039	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv907868	chr17:19768924-20217122	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	esv2763158	chr17:19777544-19789227	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19787400-19792800	Weak transcription	Fetal Heart	heart

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