Variant report

Variant	rs12968299
Chromosome Location	chr18:39007444-39007445
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs11082228	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11875240	0.89[EUR][1000 genomes]
rs11876215	0.93[EUR][1000 genomes]
rs11877923	0.80[EUR][1000 genomes]
rs12373193	0.94[EUR][1000 genomes]
rs12956831	0.91[EUR][1000 genomes]
rs12956896	0.91[EUR][1000 genomes]
rs12963842	0.93[EUR][1000 genomes]
rs1496819	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16974379	0.80[EUR][1000 genomes]
rs16974401	0.80[EUR][1000 genomes]
rs1845925	0.93[EUR][1000 genomes]
rs1942072	1.00[ASN][1000 genomes]
rs2587614	1.00[ASN][1000 genomes]
rs2587617	1.00[ASN][1000 genomes]
rs2587630	1.00[ASN][1000 genomes]
rs2587631	1.00[ASN][1000 genomes]
rs2587640	1.00[ASN][1000 genomes]
rs2587641	1.00[ASN][1000 genomes]
rs2587643	1.00[ASN][1000 genomes]
rs2587644	1.00[ASN][1000 genomes]
rs2587645	1.00[ASN][1000 genomes]
rs2587646	1.00[ASN][1000 genomes]
rs2587647	1.00[ASN][1000 genomes]
rs2612320	1.00[ASN][1000 genomes]
rs2612321	1.00[ASN][1000 genomes]
rs2612322	1.00[ASN][1000 genomes]
rs2612337	1.00[ASN][1000 genomes]
rs2612341	1.00[ASN][1000 genomes]
rs2612345	1.00[ASN][1000 genomes]
rs2612346	1.00[ASN][1000 genomes]
rs2612347	1.00[ASN][1000 genomes]
rs2612349	1.00[ASN][1000 genomes]
rs2612350	1.00[ASN][1000 genomes]
rs2612351	1.00[ASN][1000 genomes]
rs2703163	0.91[EUR][1000 genomes]
rs2703169	1.00[ASN][1000 genomes]
rs2703170	1.00[ASN][1000 genomes]
rs2848747	1.00[ASN][1000 genomes]
rs2848748	1.00[ASN][1000 genomes]
rs2848757	1.00[ASN][1000 genomes]
rs2848769	1.00[ASN][1000 genomes]
rs2848784	0.91[EUR][1000 genomes]
rs34177537	1.00[ASN][1000 genomes]
rs34298584	0.89[EUR][1000 genomes]
rs34736827	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34817685	1.00[ASN][1000 genomes]
rs4404160	1.00[ASN][1000 genomes]
rs58843487	0.93[EUR][1000 genomes]
rs58876223	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6507417	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66959060	1.00[ASN][1000 genomes]
rs7238489	1.00[ASN][1000 genomes]
rs7238895	1.00[ASN][1000 genomes]
rs7239092	0.80[EUR][1000 genomes]
rs72903956	1.00[ASN][1000 genomes]
rs72903960	1.00[ASN][1000 genomes]
rs72903968	1.00[ASN][1000 genomes]
rs72903976	1.00[ASN][1000 genomes]
rs72903977	1.00[ASN][1000 genomes]
rs72903981	1.00[ASN][1000 genomes]
rs72903999	1.00[ASN][1000 genomes]
rs72905909	1.00[ASN][1000 genomes]
rs72905919	1.00[ASN][1000 genomes]
rs72905927	1.00[ASN][1000 genomes]
rs72905935	1.00[ASN][1000 genomes]
rs72905937	1.00[ASN][1000 genomes]
rs72905973	1.00[ASN][1000 genomes]
rs72905981	1.00[ASN][1000 genomes]
rs72905986	1.00[ASN][1000 genomes]
rs72905989	1.00[ASN][1000 genomes]
rs72907804	1.00[ASN][1000 genomes]
rs72907808	1.00[ASN][1000 genomes]
rs72907817	1.00[ASN][1000 genomes]
rs72907821	1.00[ASN][1000 genomes]
rs72907842	1.00[ASN][1000 genomes]
rs72907845	1.00[ASN][1000 genomes]
rs72907847	1.00[ASN][1000 genomes]
rs72907850	1.00[ASN][1000 genomes]
rs72907851	1.00[ASN][1000 genomes]
rs72907853	1.00[ASN][1000 genomes]
rs72907854	1.00[ASN][1000 genomes]
rs72907855	1.00[ASN][1000 genomes]
rs8098315	1.00[ASN][1000 genomes]
rs8098394	1.00[ASN][1000 genomes]
rs9675507	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv909564	chr18:38739067-39179256	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1066869	chr18:38742896-39680723	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv543685	chr18:38742896-39680723	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv833630	chr18:38817119-39012222	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	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	chr18:39007400-39008800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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